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Results 1 - 10 of 11 for Gonadal dysgenesis
  1. Perrault syndrome 
    ... not show signs and symptoms of the condition. Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance Gonadal dysgenesis with sensorineural deafness, autosomal recessive inheritance Gonadal dysgenesis, ...
    https://medlineplus.gov/genetics/condition/perrault-syndrome - Genetics
  2. Turner syndrome 
    Turner syndrome is a chromosomal condition that affects development. Females typically have two X chromosomes, but in individuals with Turner syndrome, one ...
    https://medlineplus.gov/genetics/condition/turner-syndrome - Genetics
  3. Sudden infant death with dysgenesis of the testes syndrome 
    Sudden infant death with dysgenesis of the testes syndrome (SIDDT) is a rare condition that is fatal in the first year of life; its major features include abnormalities ...
    https://medlineplus.gov/...th-with-dysgenesis-of-the-testes-syndrome - Genetics
  4. Swyer syndrome 
    ... Swyer syndrome is also called 46,XY complete gonadal dysgenesis; the medical term “dysgenesis” means "abnormal development."Swyer ... the condition. 46,XY CGD 46,XY complete gonadal dysgenesis 46,XY sex reversal Gonadal dysgenesis, 46,XY ...
    https://medlineplus.gov/genetics/condition/swyer-syndrome - Genetics
  5. Noonan syndrome 
    ... cell is sufficient to cause the disorder. Familial Turner syndrome Female pseudo-Turner syndrome Male Turner syndrome Noonan's syndrome Noonan-Ehmke syndrome NS Pseudo- ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  6. Denys-Drash syndrome 
    ... typical male chromosome pattern (46,XY), they have gonadal dysgenesis, in which external genitalia do not look clearly ... of these organs leads to diffuse glomerulosclerosis and gonadal dysgenesis, which are characteristic of Denys-Drash syndrome. Abnormal ...
    https://medlineplus.gov/genetics/condition/denys-drash-syndrome - Genetics
  7. Hereditary neuralgic amyotrophy 
    ... BM, Hoskote SS, Spinner RJ, Klein CJ. Parsonage-Turner Syndrome and Hereditary Brachial Plexus Neuropathy. Mayo Clin Proc. ...
    https://medlineplus.gov/.../hereditary-neuralgic-amyotrophy - Genetics
  8. Frasier syndrome 
    ... typical male chromosome pattern (46,XY), they have gonadal dysgenesis, in which external genitalia do not look clearly ...
    https://medlineplus.gov/genetics/condition/frasier-syndrome - Genetics
  9. Léri-Weill dyschondrosteosis 
    ... childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndrome. J Pediatr. 2005 Oct;147(4):499-507. ...
    https://medlineplus.gov/.../condition/leri-weill-dyschondrosteosis - Genetics
  10. Critical congenital heart disease 
    ... of these genetic conditions, such as Down syndrome, Turner syndrome, and 22q11.2 deletion syndrome, result from changes ...
    https://medlineplus.gov/.../critical-congenital-heart-disease - Genetics
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