Congenital disorders


Understanding congenital disorders in Ayurveda and contemporary research

Congenital disorders are disabilities or malformations present at or before birth. These are identified in prenatal life or at birth, or many years later. As per the World Health Organization, congenital anomalies are a leading cause of neonatal deaths. Every year an estimated 295 000 newborns die within 28 days of birth due to congenital anomalies. These can contribute to long-term disability, with significant impacts on individuals, families, healthcare systems, and societies. [1]
Human genetics studies individual genes, their role and function in disease, and their mode of inheritance. Genomics refers to an organism's entire genetic information, the genome,and the function and interaction of DNA within the genome, as well as with environmental or nongenetic factors such as a person's lifestyle. Characterization of the human genome in genomic studies has supported genetics to elucidate the etiology, pathogenesis of the disease, and improve therapeutic interventions and outcomes. The impressive advances in genetics, genomics, and health care information technology have significantly increased the wealth of knowledge. It is helpful in medical practice and play a prominent role in the diagnosis, prevention, and treatment of disease.[2]
The ancient rishis of Ayurveda had recognized the genetic basis of diseases. They have documented the knowledge in various contexts. The current medical system focuses on the identification of genes responsible for diseases. At the same time, the references found in Ayurveda texts indicate the causes of genetic disorders and their role in health and diseases. A proper study to bridge the gaps and connect these two pools of information can reveal significant insights for a comprehensive understanding of why and what of congenital and genetic disorders. The present article describes congenital disorders in Ayurveda texts and contemporary research.

Section/Chapter/topic Sharira / Garbha / Congenital disorders
Authors Anagha S.1, Deole Y.S.1
Reviewers Basisht G.1, Chavan- Gautam P.2
Editor Basisht G.1

1Charak Samhita Research, Training and Development Centre, I.P.G.T.& R.A., Jamnagar,

2 Center for Complementary & Integrative Health, Savitribai Phule Pune University, Maharashtra, India.
Correspondence email
Publisher Charak Samhita Research, Training and Development Centre, I.T.R.A., Jamnagar, India
Date of first publication: July 21, 2021
DOI 10.47468/CSNE.2021.e01.s09.068

Congenital disorders as per Ayurveda

In Ayurveda, the congenital disorders are considered incurable(asadhya) with poor prognosis. Similarly, some hereditary of familial (kulaja) ailments are also explained as incurable.

E.g. Congenital or hereditary obstinate urinary diseases including diabetes (Jataja prameha) [Cha. Sa. Chikitsa Sthana 6/57]

Ayurveda emphasizes on prevention of congenital disorders through proper preconception, ante- natal and intra partum care. The causes for congenital disorders are explained in detail. These are helpful in taking necessary actions to avoid such risk factors and obtaining a healthy progeny.

Causes of Congenital Disorders

Image 1:Causes of Congenital Disorders

The causes of congenital disorders can be analyzed in view of physical, mental and spiritual dimensions.

These causes can be broadly classified based on period:

1) Preconception period

2) Antenatal period

3) Intra-partum period

Factors related to preconception Period

Physical factors

Genetic defects in parents

Abnormalities in gametes (beeja dosha)

The concept of genetics is denoted with the terms ‘beeja’(seed or gametes), ‘beejabhaga’ (chromosomes) and beeja-bhagavayava (nucleic acids and genes). The maternal (matruja) and paternal (pitruja) factors are responsible for the formation of the embryo. When any part of these three genetic materials is abnormal, it leads to deformity or mal-formation of the organ or body part. [Cha. Sa. Sharira Sthana 3/17]

Role of reproductive physiology (shukra dhatu) of parents

The vitiation of reproductive elements shukra dhatu and its channels of transformation and transportation (shukravaha srotasa) results in deformities in progeny. [Cha. Sa. Sutra Sthana 28/28], [Cha. Sa. Chikitsa Sthana 2;8/34] The normal status of shukra dhatu at the time of conception is important for normal embryogenesis.

Disorders of female reproductive system

Optimum health of uterus/female reproductive tract (kshetra) is an essential factor for the normal growth and development of the fetus.

Role of time factor (kala)

Age of the parents at the time of conception is important. In Ayurvedic texts, the minimum age for normal and healthy conception is described as twenty five years for male and sixteen years for female. At this age, the individual attains complete psycho-sexual maturity to become responsible parents. [Su. Sa. Sutra Sthana 35/13] Young girls and old women are not advised for conception. [Cha. Sa. Sharira Sthana 8/6] If the recommended age is not followed for conception, it can lead to intrauterine death of fetus, neonatal death, ill health and deformed body parts of the child.[A. S. Sharira Sthana 1/5]

Pregnancy at a very young age causes premature births. Aneuploidy (abnormal chromosome number) is the principal hereditary abnormality associated with age of either parent. Advanced maternal age is associated with increased risks for miscarriage, chromosomal abnormalities, stillbirth, foetal growth restriction and preterm birth.[3]Recent research shows that younger paternal age(< 20 years) could increase the risks of urogenital abnormalities and chromosome disorders in fetus. Advanced paternal age (≥ 40 years) could increase the risks of cardiovascular abnormalities, facial deformities, urogenital abnormalities, and chromosome disorders in their offspring.[4] Growing evidences also indicate that the offspring of older fathers are prone to reduced fertility and an increased risk of birth defects, some cancers, and schizophrenia.[5]

Psychological and behavioral factors

A pleasant state of mind is the prime requirement for conception. [Cha. Sa. Sutra Sthana 25/40] The mental status of parents during coitus and conception is important. Coitus shall be avoided, when either of the partners is hungry, thirsty, or frightened, averse, sorrow-stricken, angry, distressed with relationship, or not desiring for sex. These states during coitus adversely affect conception and health of progeny. [Cha. Sa. Sharira Sthana 8/17] Studies show that preconception stress alters offspring development in a parental and fetal sex-specific manner. This is reflected in the metabolic and immune-related genes in the placenta as well as brain transcriptome.[6]

Spiritual factors

Sinful acts and atheistic attitude of parents [Su. Sa. Sharira Sthana 2/50-52], deeds of previous life (atma –karma dosha) [Cha. Sa. Sharira Sthana 2/29] and unrighteousness(adharma) [Su. Sa. Sharira Sthana 3/36] can cause congenital disorders. These factors are commonly considered as of ‘unknown origin’ in current medical practices.

Factors related to antenatal period

Improper antenatal care and poor nutrition during pregnancy can lead to deformity in the fetus. [Cha. Sa. Sharira Sthana 4/30] The six factors responsible for embryogenesis play an important role in the causation of congenital disorders. These include maternal (matruja), paternal (pitruja), spiritual (atmaja), psychological (sattvaja), adaptations (satmyaja) and nutritional component (rasaja). Minor defects in these factors can cause congenital abnormalities in the fetus. Major defects cause abortion or intrauterine death of the fetus. [Cha. Sa. Sharira Sthana 4/28-29]

Role of panchamahabhuta

The five fundamental elements (pancha mahabhuta) play basic functions during embryogenesis. Vayu performs function of cell division/multiplication (vibhajana); agni carries function of metabolism(pachana); jala carries function of moisture or fluid (kledana); Prithvi carries function of compactness or formation of mass(samhanana); and akasha carries function of enlargement of size(vivardhana). If these functions are carried out in normal proportion, the body's normal structure (shareera) is formed. The defective proportion or functioning can adversely affect embryogenesis and result in congenital anamolies. [Su.Sa. Sharira Sthana 5/3] More specifically, vayu and akasha cause anatomical deformities in children. [Bhela Sa Sharira Sthana 3/15-16]

Role of dosha

Vitiation of all three dosha during pregnancy can cause congenital disorders. [A. H. Sharira Sthana 1/6] Vata dosha plays key role as controller of all activities and anatomical shapes (akruti) of the embryo (garbha). [Cha. Sa. Sutra Sthana 12/8], [Su. Sa. Sharira Sthana 2/50-52]

Role of dhatu

The structural and functional integrity of maternal reproductive organs especially the uterus is having a great role in the growth and development of the fetus. The quality of rasa dhatu of the mother and its transportation to the fetus plays a vital role.The placenta (apara) and umbilical cord (nabhi nadi) also play crucial role in the nourishment of fetus (garbha poshana). The disorder of these structural entities certainly affects the fetus and leads to some congenital deformities.

Mental status of mother

The mental status of the mother during pregnancy can influence fetal growth and development.The psychological and cognitive development of fetus depends on the psychological status of the mother and the topics listened to by the pregnant woman.[A.S. Sharira Sthana 1/66] And also, the importance of maintaining the positive psychological status of mother while treating the fetal growth related ailments like intra uterine growth restriction is being emphasized.[A.H. sharira Sthana 2/20]

Diet and lifestyle of the mother

The harmful diet and lifestyle factors followed by mothers that can adversely affect progeny (garbhopaghatakara bhavas) are described below. [Cha. Sa. Sharira Sthana 8/21] More research studies are needed to find out exact genetic connections in the causes and their effects on progeny.

Causes of premature birth or atrophy or emaciation of fetus

  • Sitting in awkward positions, on uneven and hard seats
  • Suppressing the urge to pass flatus, urine, and defecation
  • Indulgence in intensive or extreme forms of physical activities
  • Excessive consumption of pungent and hot food items or less quantity of food than needed

Causes of miscarriage

  • Repeated trauma or injuries, looking down from heights (e.g., from mountain-tops or cliffs, deep wells, etc.)
  • Traveling long distances in excessively jerky carriages
  • Prolong exposure to loud and unpleasant noise

Causes of mental retardation and psychiatric disorders in child

  • Excess sleeping in open air or walking at night leads to the birth of a mentally challenged child.
  • Indulgence in too many quarrels and fights can lead to epilepsy in a child.
  • Excess indulgence in coitus (or a nymphomaniac) leads to the birth of a truant with a passion for women.
  • Constant grief in pregnancy would give birth to a timid, or under-developed, or short-lived child.
  • A woman who always thinks ill of others gives birth to a delinquent or an anti-social child.
  • A woman who is a thief will give birth to a lazy child who is wicked and inept.
  • An intolerant woman would give birth to a child who is of fierce, deceitful, and jealous nature.

Lifestyle-related causes

  • A woman who sleeps for long hours would give birth to a dull and unwise child with poor digestive capacity.
  • A woman addicted to wines gives birth to a child who is ever-thirsty and fickle-minded.

Dietary causes

  • A woman who consumes flesh and meat of godha (iguana) would give birth to a child afflicted with stones or shanairmeha (a type of urinary disorder where dribbling is seen)
  • A woman who consumes pork frequently would give birth to a child with red eyes, rough body-hair, and prone to suffering from severe respiratory disorders.
  • A woman who used to consume fish excessively would give birth to a child with lagophthalmos and related eye disorders
  • A woman used to eating many sweets is prone to giving birth to a dumb or excessively obese child or a diabetic child.
  • A woman fond of sour food items is prone to giving birth to an offspring suffering from bleeding disorders or diseases of the skin and eyes.
  • A woman who consumes more salt or salty food articles may give birth to a child with early onset of wrinkles, grey hair, or baldness.
  • A woman used to pungent substances in excess may give birth to a weak child, deficient in semen and impotent.
  • A woman using bitter substances in excess may give birth to a child with emaciated, weak or undeveloped body.
  • A woman habituated to excessive use of astringents may give birth to a child with a blackish complexion, suffering from constipation and udavarta (misperistalsis).

[Cha.Sa. Sharira Sthana 8/21]

The effect of diet taken by the mother vitiating particular dosha is described. [A. S. Sharira Sthana 2/54-56]

A systematic review shows that parental alcohol exposures are significantly associated with the risk of congenital heart diseases in offspring. This highlights the necessity of improving health awareness to prevent alcohol exposure during preconception and conception periods.[7]

Effect of maternal diseases upon the fetus

The affliction of the body part of the pregnant woman, either by vitiation of dosha or trauma, leads to the affliction of the identical part of the fetal body. [ Su. Sa. Sharira Sthana 3/17] Maternal autoantibodies can cross the placenta and cause fetal damage. For example, fetal thyroid goiter can be developed in response to maternal Graves' disease.[8]

Effect of non-fulfillment of longings/desires of the mother during pregnancy (dauhruda vimanana)

The fetus expresses desires through mother. Hence the desires of the pregnant woman (dauhruda) should always be fulfilled. Any negligence or non-fulfillment can cause abnormalities or even death of the fetus. Suppression of desires vitiates vayu, and produces various diseases, abnormalities in the fetus, or even death. [Cha. Sa. Sharira Sthana 4/25] Various studies indicate that mental illness and neurocognitive decline are prevalent co-morbidities in the adolescent and adult population with congenital heart diseases (CHD).[9] [10]

Environmental factors

Environmental conditions can play a role in fetal development. A retrospective cohort study reported a significant positive association between soil cadmium and air pollution evaluated by air quality index (AQI) and level of screening serum TSH in congenital hypothyroidism patients. It is inferred that the interaction of genetic, autoimmune, familial, and environmental factors with each other could have an influence on neonatal thyroid function.[11]

Factors related to intra partum period

Consequences of inappropriate bearing down efforts by the mother: If bearing down efforts are made in the absence of real labour pains, deafness, dumbness, dislocation of mandible, head and neck diseases, cough, dyspnoea, emaciation, and abnormal location of the body parts of the child are likely to occur. [ Su. Sa. Sharira Sthana 10/9]

Classification of congenital disorders

The congenital disorders are classified in two major categories. [ Su. Sa. Sutra Sthana 24/5]

1) Due to genetic defects (aadibalapravrutta):

These include maternal (matruja) or paternal (pitruja) genetic factors. These can be termed as ‘pre-conception causes’.


  • Skin lesions (kushtha): Skin lesions resembling the petal of lotus(pundarika), fruit of Abrus pricatorius (kakanaka)[Su. Sa. Nidana Sthana 5/19] and congenital skin patches of different size, shape and colour.[Su. Sa. Nidana Sthana 13/41-44]
  • Hemorrhoids (arsha)[ Su. Sa. Sutra Sthana 24/5]
  • Obstinate urinary disorders (prameha)[ Su. Sa. Sutra Sthana 24/5]
  • Emaciation (karshya/kshaya) [Dalhana, Su. Sa. Sutra Sthana 24/5]
  • Shandi yoni vyapad (female without sexual desire and undeveloped breasts) is caused due to abnormalities in male and female gametes (beeja dosha) and affliction of the uterus by vitiated vata dsoha. [Cha. Sa. Chikitsa Sthana 30/34-35] This condition is similar to the chromosomal disorder known as “Turner’s syndrome”.
  • The defects in the sperm (shukra) cause deformities in factors related to paternal origin. [Cha. Sa. Sharira Sthana 4/30-31]

2) Disorders due to faulty diet and lifestyle habits of mother, especially during the prenatal period (janmabalapravrutta):

These may be either due to nutritional factors (rasakruta) or psychological factors (duahruda apacharakruta). These can be termed as ‘post-conception causes’.


  • Limb deformities (pangu)
  • Congenital blindness (jatyandhya)
  • Deafness (badhira)
  • Dumbness (mooka)
  • Nasal voice (minmina)
  • Dwarfism (vaamana)

The following table shows comprehensive information about genetic disorders and their consequences on progeny.

Gender Vitiated factor Outcome Possible modern co-relation
Female Genes in maternal chromosomes(beejabhaga of shonita), responsible for the formation of uterus(garbhashaya) female not capable of reproduction, infertile female(vandhya) Agenesis of uterus/adnexa leading to infertility
Female Some of the DNA bases (beejabhaga avayava) in the genes of maternal chromosomes responsible for the formation of uterus (garbhashaya) can conceive, but deliver only dead fetus (putipraja) Recurrent pregnancy loss due to genetic disorders.
Female Some of the DNA bases(beejabhaga avayva) in the genes of maternal chromosomes responsible for the formation of uterus (garbhashaya) as well as those responsible for developing feminine characters incomplete female/ transgender (varta) Gonadal dysgenesis Eg:-Turner Syndrome,Swyer Syndrome
Male Genes in paternal chromosomes(beejabhaga of shukra), responsible for the formation of sperms(shukra) sterile male (vandhya) Male Infertility due gonadal agenesis
Male Some of the DNA bases(beejabhaga avayva) in the genes of paternal chromosomes responsible for the formation of sperms(shukra) offspring dies after delivery (putipraja) Recurrent pregnancy loss due to genetic disorders
Male Some of the DNA bases (beejabhaga avayava) in the genes of paternal chromosomes responsible for the formation of sperms(shukra) as well as those responsible for developing masculine characters. incomplete male /transgender (trinaputrika) Gonadal dysgenesis

Some genetic conditions are caused by mutations in only a single gene. These conditions are usually inherited in different patterns, depending on the type of gene.

The following table shows some examples.

Pattern of inheritance Description Example
X-linked dominant *By mutations in genes on the X chromosome,
  • In females, a mutation in one of the two copies of the gene in each cell is sufficient to cause the disorder.
  • In males, a mutation in the only copy of the gene in each cell causes the disorder.
  • In most cases, males experience more severe symptoms of the disorder than females.
fragile X syndrome
X-linked recessive * Caused by mutations in genes on the X chromosome.
  • A mutation would have to occur in both copies of the gene to cause the disorder in females.
  • In males, one altered copy of the gene in each cell is sufficient to cause the condition.
  • Males are affected by X-linked recessive disorders much more frequently than females.
hemophilia, Fabry disease
Y-linked * Caused by mutations in genes on the Y chromosome.
  • So, the mutation can only be passed from father to son.
Y chromosome infertility, some cases of Swyer syndrome
Autosomal dominant * One mutated copy of the gene in each cell is sufficient for a person to be affected.
  • An affected person can inherit the condition from an affected parent.
  • the condition may result from a new mutation in the gene (e, without any family history)
Huntington disease, Marfan syndrome
Autosomal recessive * Both copies of the gene in each cell should have mutations.
  • Typically not seen in every generation of an affected family.
cystic fibrosis, sickle cell disease
Codominant * Two different versions (alleles) of a gene are expressed.
  • Both alleles influence the genetic trait or determine the characteristics of the genetic condition.
ABO blood group, alpha-1 antitrypsin deficiency
Mitochondrial * Also known as maternal inheritance
  • Applies to the genes in mitochondrial DNA
  • Only females can pass on mitochondrial mutations to their children as only egg cells contribute mitochondria to the developing embryo.
Leber hereditary optic neuropathy (LHON)

Many health conditions are caused by the combined effects of multiple genes which are known as polygenic. It may be by the interactions between genes and the environment also. For example, heart disease, type 2 diabetes, schizophrenia, certain types of cancer etc.[12]

Diagnosis of Congenital disorders

History of parents

A careful history of either several spontaneous abortions or offspring with multiple anomalies is an indication for chromosome analyses on both parents. Among known genetic disorders, the severity of X-linked disorders differs in males and females. Genetic mutations originate more frequently among males, and the frequency increases with advancing paternal age. This is seen in Marfan syndrome, achondroplasia, hemophilia A, and the Lesch-Nyhan syndrome.[13] The genetic analyses in such cases can diagnose probable genetic disorders in progeny.

Check up before pregnancy:

The genetic diseases like cystic fibrosis, fragile X syndrome, sickle cell disease, Tay-Sachs disease, Spinal muscular atrophy can be identified in carrier parents before pregnancy. It can also be done in high-risk category parents who are susceptible to disorders due to ethnicity. Common susceptible groups that may be carriers include non-Hispanic whites (cystic fibrosis), people of Eastern European Jewish descent (Tay-Sachs disease, cystic fibrosis, and others), and those of African, Mediterranean, and Southeast Asian backgrounds (sickle cell disease). [14]

During pregnancy:

The risk of Down syndrome, trisomy 18, and spine and brain problems can be diagnosed between 10 and 13 weeks of pregnancy by check up. The cell free fetal DNA testing, AFP (alphafetoprotein) test, Maternal serum quad screen, Amniocentesis and Chorionic Villus Sampling (CVS) are done in susceptible cases.

Antenatal anomaly scan:

An anomaly scan or mid-pregnancy scan is done to detect significant physical abnormalities in the growing baby. It is an ultrasound scan done between the 18th and 21st week of pregnancy. It helps detect congenital disorders like anencephaly, diaphragmatic hernia, gastroschisis, exomphalos, open spina bifida, bilateral renal agenesis, lethal skeletal dysplasia, Edwards’ syndrome or T18, Patau’s syndrome or T13, cleft lip and serious cardiac abnormalities.[15]

Clinical examination

Clinical diagnosis of congenital disorders is based on the three-fold diagnostic tools.

1) Inspection (darshana): A careful neonatal examination after birth can identify visible structural deformities. The examination findings in each part of the neonate body for the signs which indicate life span. [Cha. Sa. Sharira Sthana 8/51]

2) Palpation (sparshana): Any structural deformity or anatomical abnormality can be easily detected by palpation. [Cha. Sa. Sharira Sthana 8/43], [A.Hr. Uttara Sthana 1/1]

3) Interrogation (prashna): The detailed history of both the parents regarding the family history, personal history, medical history should be taken to rule out or to find the cause of a congenital disorder in the child. It can be useful in diagnosis and prevention of hereditary disorders.


Most of congenital disorders are incurable. The patients shall be well informed about the prognosis before treating such diseases. The measures to minimize the symptoms of the particular disorder and improve the quality of life should be the goal of treatment.

Surgical procedures:

Some surgical or para surgical measures are advised in case of minor structural deformities like Stricture of uretra (nirudha prakasha)[Su. Sa. Nidana Sthana 13/52-54] and imperforate anus (sannirudha gudam) [Su. Sa. Nidana Sthana 13/55-56]. The description of the surgical procedure is also available for the treatment of these congenital disorders.[Su. Sa. Chikitsa Sthana 20/43-47]

In congenital skin patches that are small,round, painless, slightly raised, light red coloured and smooth (known as jatumani), blackish, minute as in sesame seed size (tilakalaka)etc. cauterization using caustic alkali(kshara karma) or thermal cauterization (agnikarma) is advised.[Su. Sa. Chikitsa Sthana 20/32]

In other skin changes, which are circular in shape, covering a large or small area, bluish black or white in colour (known as nyaccha), bloodletting therapy (sira vyadha) as per convenience is advised. [Su. Sa. Chikitsa Sthana 20/33]

Preventive aspects of congenital disorders

Pre-conception guidelines are recommended for healthy progeny and to prevent congenital disorders. The guidelines include the selection of partners, purification procedures, and prenatal care.

Guidelines for selection of partner

The selection of a partner with desirable qualities is the prime step in the prevention of congenital disorders. The following are the guidelines for the selection of an ideal partner as per Ayurveda text.

  • The partner should belong to a different clan (gotra).[ Cha. Sa. Sharira Sthana 2/3]
  • Consanguinity in sexual relationships should be avoided.
  • Either partner should not have any hereditary disorders or familial traits.
  • Either partner should not be suffering from any contagious or sexually transmitted diseases.
  • Either partner should not be handicapped.
  • Both should possess attractive physical characters.
  • Both partners should be healthy and follow good health habits.
  • Both should follow good morals and conduct. [A. S. Sharira Sthana 1/3]

These guidelines are essential to prevent the transmission of genetic disorders in the family.

Preventive and therapeutic protocol

If either the parents or both of them have any hereditary disorders, the therapies are advised. Panchakarma procedures including therapeutic purgation (virechana) followed by administration of rasayana and vajikarana therapy can help to prevent or minimize genetic disorders in progeny. Suppose the first child is born with any kind of congenital disorder. In that case, the preventive protocol must be followed before planning for the next baby.

Current research

Contemporary approach:

As per modern embryology, susceptibility to teratogenesis depends on the genotype of the conceptus and the manner in which this genetic composition interacts with the environment. The maternal genome is also important with respect to drug metabolism, resistance to infection, and other biochemical and molecular processes that affect the conceptus. Susceptibility to teratogens varies with the developmental stage at the time of exposure.

The most sensitive period for inducing congenital disabilities is the third to eight weeks of gestation, the period of embryogenesis.[16]

There are three phases of intrauterine growth. Zygote, embryo, and fetus.

1. The zygote phase or Period-I (weeks 1 – 2 after fertilization): It consists of cell division and implantation of this cell mass in the uterus. During this phase, teratogen would cause loss of the conceptus.

2. The embryonic phase or Period II (weeks 3 – 8): In this period, most of the organ systems develop. This is the most vulnerable phase for major congenital malformations to occur.

3. The fetal phase / Period III (weeks 9 – 38): In this phase, further growth and elaboration of the organ systems take place. During this phase, various factors can result in minor or not-so-severe defects.

Congenital disabilities occur due to three main reasons i.e.abnormal formation of tissues, abnormal forces on normal tissues, or destruction of normal tissues. Some of these defects may have a cascade effect and result in related anomalies or multiple anomalies (syndromes).[17]

Nowadays, allogeneic hematopoietic stem cell transplantation (allo-HSCT) is emerging as a treatment of choice for various congenital disorders.[18]

Theses works done

1. M.N. Jaiswal (2003): Clinical role of indigenous drugs (Amalaki Rasayana and Gomeda Bhasma) in Kulaja Pandu (Thalassemia)-A scientific study, Dept. of Kaumarabhrutya., Shree Ayurved Mahavidhyalaya, Nagpur.

2. Ruchi Singh (2007): A study of disease Thalassemia (Anukta Vyadhi Ayurveda) and its management with Dhatri Avaleha, Department of Kaumarabhrutya, I.PG.T & R.A, Jamnagar.

3. Jadhav Sahebrao B (2009): A study of disease Thalassemia (Anukta Vyadhi in Ayurveda) and its management with Triphaladi Avaleha as an adjuvant therapy, Department of Kaumarabhrutya, I.PG.T & R.A, Jamnagar.

4. Joban K. Modha (2009): A comparative pharmaco-pharmaceutical clinical study of Gandhakadi Yoga B on Iron overloading condition due to Raktavikruti, Deprtment of RSBK, I.PG.T & R.A, Jamnagar.

5. Pramod R. Yadav (2010): The pharmaceutical standardization of Gandhakadi Yoga and its effect on Thalassemic iron overload w.s.r. to Kadli as pathya, Deprtment of RSBK, I.PG.T & R.A, Jamnagar.

6. Sagar Nalawade (2011): Pharmacological study of Amritasara Lohokta Dosha Nivaraka Dravya on iron overloading with special reference to Thalassemia Major, NIA, Jaipur.

7. Abhishek Y. Patalia (2011): A study of Beejadushtijanya Pandu and its management with Triphaladi Avaleha w.s.r. to Thalassemia, Department of Kaumarabhrutya, I.PG.T & R.A, Jamnagar.

8. Raina Rathod (2013): A further clinical study on Beejadushtijanya Pandu- Thalassemia Major and with Triphaladi Avaleha, Department of Kaumarabhrutya, I.PG.T & R.A, Jamnagar.

9. Shailesh R. Rajgolkar (2014): A clinical study on Beejadushtijanya pandu (Thalassemia major) in children and its management with Musta-Triphaladi Avaleha, Department of Kaumarabhrutya, I.PG.T & R.A, Jamnagar.

10. Anjana A. goswami ( 2015) : A clinical study on Beejadushtijanya pandu (Thalasemia major) and its management with Gandhakadi yoga, Department of Kaumarabhrutya, I.PG.T & R.A, Jamnagar.

11. O.T.M.R. Senani B kalawana (2016 ) : Management of Beejadushtijanya pandu(Thalasemia major) with Musta-triphladi avaleha and gandhkadi yoga, Department of Kaumarabhrutya, I.PG.T & R.A, Jamnagar.

12. Rahul Gameti (2017): Further clinical study on Beejadushtijanya pandu (Thalasemia major)and its management with Gandhakadi yoga, Department of Kaumarabhrutya, I.PG.T & R.A, Jamnagar.

13. Bhumi Mori(2018) : Management of Beejadushtijanya Pandu (Thalassemia Major) with modified Musta-Triphaladi Avaleha and Gandhakadi Yoga: An Open Labelled, Randomized, Controlled, Clinical Trial , Department of Kaumarabhrutya, I.PG.T & R.A, Jamnagar.

More information

Atulyagotriya Sharira , Khuddika Garbhavakranti Sharira, Mahatigarbhavakranti Sharira, Jatisutriya Sharira , Yonivyapat Chikitsa Adhyaya, Garbha, Prenatal care (garbhini paricharya)

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  1. Available from accessed on 15/06/2021
  2. J. Larry Ja meson, Peter Kopp. Principles of Human Genetics. In Harrison’s principles of internal medicine. 19th edition. Pg. 425.
  3. Frick AP. Advanced maternal age and adverse pregnancy outcomes. Best Pract Res Clin Obstet Gynaecol. 2021 Jan;70:92-100. doi: 10.1016/j.bpobgyn.2020.07.005. Epub 2020 Jul 15. PMID: 32741623.
  4. Fang Y, Wang Y, Peng M, et al. Effect of paternal age on offspring birth defects: a systematic review and meta-analysis. Aging (Albany NY). 2020;12(24):25373-25394. doi:10.18632/aging.104141
  5. Bray I, Gunnell D, Davey Smith G. Advanced paternal age: how old is too old?. J Epidemiol Community Health. 2006;60(10):851-853. doi:10.1136/jech.2005.045179
  6. Yasmine M.Cissé et al, Brain and placental transcriptional responses as a readout of maternal and paternal preconception stress are fetal sex specific, Placenta, Volume 100, October 2020, Pages 164-170.
  7. Zhang S, Wang L, Yang T, Chen L, Zhao L, Wang T, Chen L, Ye Z, Zheng Z, Qin J. Parental alcohol consumption and the risk of congenital heart diseases in offspring: An updated systematic review and meta-analysis. Eur J Prev Cardiol. 2020 Mar;27(4):410-421. doi: 10.1177/2047487319874530. Epub 2019 Oct 2. PMID: 31578093.
  8. Panaitescu AM, Nicolaides K. Maternal autoimmune disorders and fetal defects. J Matern Fetal Neonatal Med. 2018;31(13):1798‐1806. doi:10.1080/14767058.2017.1326904
  9. Khanna AD, Duca LM, Kay JD, Shore J, Kelly SL, Crume T. Prevalence of Mental Illness in Adolescents and Adults With Congenital Heart Disease from the Colorado Congenital Heart Defect Surveillance System. Am J Cardiol. 2019;124(4):618‐626. doi:10.1016/j.amjcard.2019.05.023
  10. Keir M, Ebert P, Kovacs AH, et al. Neurocognition in Adult Congenital Heart Disease: How to Monitor and Prevent Progressive Decline. Can J Cardiol. 2019;35(12):1675‐1685. doi:10.1016/j.cjca.2019.06.020
  11. Hashemipour, M., Kelishadi, R., Amin, M.M. et al. The association between familial and environmental factors and prevalence of congenital hypothyroidism in center of Iran. Environ Sci Pollut Res (2020).
  13. Congenital deformities and chromosomal disorders: maternal versus paternal age. Fertil Steril. 1977;28(8):888. doi:10.1016/s0015-0282(16)42748-2
  14. Available from cited on 17/06/2021
  15. Available from cited on 17/06/2021
  16. Prof.Hari Hirdya Awasthi,Dr.Mohd.Ashraf Khan, Garbha sarira, Chaukhambha Orientalia. Varanasi; 1996. First
  17. Dhiman K, Kumar A, Dhiman KS. Shad Garbhakara Bhavas vis-a-vis congenital and genetic disorders. Ayu. 2010;31(2):175‐184. doi:10.4103/0974-8520.72384
  18. Faraci M, Giardino S, Bagnasco F, et al. Allogeneic hematopoietic stem cell transplantation in congenital disorders: A single-center experience. Pediatr Transplant. 2017;21(6):10.1111/petr.12997. doi:10.1111/petr.12997