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- Jul 21, 2019
18000096. A 46,XY mother who developed as a normal woman underwent spontaneous puberty, reached menarche, menstruated regularly, experienced two unassisted pregnancies, and gave birth to a 46,XY daughter with complete gonadal dysgenesis."
46, XY disorders of sexual development | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program
A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for 46, XY disorders of sexual development
“Infants with this condition tend to have penoscrotal hypospadias, abnormal development of the testes, and reduced to no sperm production. Some individuals with 46, XY DSD have fully to underdeveloped female reproductive organs (e.g., uterus and fallopian tubes), while others do not.[1] People with with 46, XY DSD may be raised as males or females. Treatment involves surgery and hormone replacement therapy.[1] People with 46, XY DSD are at an increased risk for gonadal tumors and benefit from regular surveillance or surgery to remove abnormally developed gonads.[1]
Last updated: 12/7/2012”
46 xy is chromosomally male.
Edited to add quotes.
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