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Results 1 - 6 of 6 for Ovarian dysgenesis 7
  1. HSD17B4 gene 
    ... Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome. Am ...
    https://medlineplus.gov/genetics/gene/hsd17b4 - Genetics
  2. Leukoencephalopathy with vanishing white matter 
    ... females may have abnormal development of the ovaries (ovarian dysgenesis). Specific changes in the brain as seen using ...
    https://medlineplus.gov/...ncephalopathy-with-vanishing-white-matter - Genetics
  3. NR5A1 gene 
    ... SUBFAMILY 5, GROUP A, MEMBER 1; NR5A1 PREMATURE OVARIAN FAILURE 7; POF7 SPERMATOGENIC FAILURE 8; SPGF8 NCBI Gene ClinVar ... K, Bashamboo A. Mutations in NR5A1 associated with ovarian insufficiency. N ... Morel Y. Gonadal dysgenesis without adrenal insufficiency in a 46, XY patient ...
    https://medlineplus.gov/genetics/gene/nr5a1 - Genetics
  4. Turner syndrome 
    ... but egg cells usually die prematurely and most ovarian tissue breaks down before birth. Many affected individuals ... percentage of people with Turner syndrome retain normal ovarian function through young adulthood.About 30 percent of ...
    https://medlineplus.gov/genetics/condition/turner-syndrome - Genetics
  5. SRY gene 
    ... syndrome, also known as 46,XY complete gonadal dysgenesis or 46,XY pure gonadal dysgenesis. Swyer syndrome is a condition that affects sex ... XY difference of sex development, or partial gonadal dysgenesis. The effects of these variants on the function ...
    https://medlineplus.gov/genetics/gene/sry - Genetics
  6. WNT4 gene 
    ... and adult ovaries and its signaling contributes to ovarian cell survival. Mol Cell Endocrinol. 2010 Apr 12; ...
    https://medlineplus.gov/genetics/gene/wnt4 - Genetics