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Results 1 - 7 of 7 for Ovarian dysgenesis 1
  1. Perrault syndrome 
    ... recessive inheritance Gonadal dysgenesis, XX type, with deafness Ovarian dysgenesis with sensorineural deafness ... PERRAULT SYNDROME 1; PRLTS1 PERRAULT SYNDROME 4; PRLTS4 PERRAULT SYNDROME 5; ...
    https://medlineplus.gov/genetics/condition/perrault-syndrome - Genetics
  2. HSD17B4 gene 
    ... deficiency. Mol Cell Endocrinol. 2001 Jan 22;171(1-2):61-70. doi: ... cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome. Am ...
    https://medlineplus.gov/genetics/gene/hsd17b4 - Genetics
  3. SRY gene 
    ... tissue from both female and male reproductive organs (ovarian and testicular tissue). ... doi: 10.1007/s00109-002-0376-9. Epub 2002 Oct 1. Citation on PubMed Delot EC, Vilain EJ. Nonsyndromic ...
    https://medlineplus.gov/genetics/gene/sry - Genetics
  4. NR5A1 gene 
    ... of sex development, also known as partial gonadal dysgenesis. Affected ... men and primary ovarian insufficiency in women, result in an inability to ...
    https://medlineplus.gov/genetics/gene/nr5a1 - Genetics
  5. WNT4 gene 
    ... MEMBER 4; WNT4 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND ... its signaling contributes to ovarian cell survival. Mol Cell Endocrinol. 2010 Apr 12; ...
    https://medlineplus.gov/genetics/gene/wnt4 - Genetics
  6. Turner syndrome 
    Turner syndrome is a chromosomal condition that affects development in people who are assigned female at birth. Females typically have two X chromosomes, but ...
    https://medlineplus.gov/genetics/condition/turner-syndrome - Genetics
  7. Leukoencephalopathy with vanishing white matter 
    ... may have abnormal development of the ovaries (ovarian dysgenesis). Specific changes in the brain ... Dietrich J, Lacagnina M, Gass D, ...
    https://medlineplus.gov/...ncephalopathy-with-vanishing-white-matter - Genetics