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16 results
  1. Perrault Syndrome - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK242617
    ... air conduction. Ovarian dysfunction in women with a 46,XX karyotype . The spectrum of ovarian dysfunction extends across a continuum from primary ovarian insufficiency (POI) to ovarian dysgenesis. POI is defined as cessation of menses before ...
  2. pdf2017MeshTreesWithChangesShown.pdf 
    https://www.nlm.nih.gov/.../2017MeshTreesWithChangesShown.pdf
    ... Adrenal Hyperplasia, Congenital Hyperandrogenism Gonadal Dysgenesis Gonadal ... Anovulation Oophoritis Ovarian Cysts Polycystic Ovary Syndrome ...
  3. xmlghr-summaries.xml 
    https://medlineplus.gov/download/ghr-summaries.xml
    ... females may have abnormal development of the ovaries (ovarian dysgenesis). Specific changes in the brain as seen using ... with Perrault syndrome have abnormal or missing ovaries (ovarian dysgenesis), although their external genitalia are normal. Severely affected ...
  4. 2019New_Mesh_Tree_Hierarchy.txt 
    https://www.nlm.nih.gov/.../download/2019New_Mesh_Tree_Hierarchy.txt
    ... Sex Development C12.706.316.064.249 Gonadal Dysgenesis, 46,XX C12.706.316.064.500 Hyperandrogenism C12.706. ... Gonadal Dysgenesis C12.706.316.309.193 Gonadal Dysgenesis, 46,XX C12.706.316.309.388 Gonadal Dysgenesis, 46, ...
  5. pdf2016MeshTree.pdf 
    https://www.nlm.nih.gov/mesh/2016/download/2016MeshTree.pdf
    ... Sex Development C12.706.316.064.249...........................................Gonadal Dysgenesis, 46,XX C12.706.316.064.500...........................................Hyperandrogenism C12.706. ...
  6. xmlTopicIndex.xml 
    https://medlineplus.gov/download/TopicIndex.xml
    ... XX type, with deafness</other_name><other_name >Ovarian dysgenesis with sensorineural deafness</other_name></other_names></topic>< ...
  7. WNT4 gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/wnt4
    ... TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 4; WNT4 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS; SERKAL Gene and ...
  8. Nonsyndromic 46,XX Testicular Disorders of Sex Development - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1416
    ... 46,XY DSD) and 46,XY complete gonadal dysgenesis (46,XY CGD) but not in individuals with a 46,XX testicular DSD. Normal gene product . SRY encodes a ...
  9. SRY gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/sry
    ... this condition have a female-typical chromosome pattern (46,XX karyotype) and tissue from both female and male reproductive organs (ovarian and testicular tissue). Other Names for This Gene ...
  10. Differences of sex development 
    https://medlineplus.gov/ency/article/001669.htm
    ... tumors in the mother. These are most often ovarian tumors. Mothers who have children with 46,XX DSD should be checked for this unless there ...
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