46, XX gonadal dysgenesis and ovarian hypoplasia. - National Genomics Data Center (CNCB-NGDC)

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46, XX gonadal dysgenesis and ovarian hypoplasia.

J Málková, R Chrz, K Motlík, L Stárka, J Kobilková, E Silinková-Málková

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PMID: 4844641 DOI: 10.1007/BF00285106

No abstract text available.

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Adolescent

Adult

Androstenedione

Congenital Abnormalities

Female

Humans

Hydroxyprogesterones

Maternal Age

Ovarian Diseases

Ovary

Pedigree

Testosterone

Turner Syndrome

Hydroxyprogesterones

Testosterone

Androstenedione

Journal Article

Familial 46,XX gonadal dysgenesis.Familial 46,XX gonadal dysgenesis.46,XX gonadal dysgenesis with epibulbar dermoid.Twins discordant for 46,XX gonadal dysgenesis.Familial ovarian dysgenesis in 46,XX females.46,XX gonadal absence: a variant of the XX pure gonadal dysgenesis?Ovarian development in 46,XY gonadal dysgenesis.Familial dysgerminoma associated with 46, XX pure gonadal dysgenesis.46,XX gonadal dysgenesis associated with congenital nerve deafness.Pure gonadal dysgenesis (46 XX type) with a familial pattern.