Ovarian development in 46,XY gonadal dysgenesis.

M H Russell, S S Wachtel, B W Davis, L T Cahill, E Groos, G D Niblack, I M Burr
Author Information

Abstract

In humans the XY ovary is degenerative, there being scant evidence of persistence of that organ beyond the perinatal period. Here we describe indications of functional ovarian tissue in a 17-year-old female with male karyotype, H-Y+ cellular phenotype, and some signs of the Turner syndrome. Her gonads were removed after the onset of secondary amenorrhea. Histological examination revealed a degenerative right ovary devoid of germ cells and follicles, and a left streak gonad. There was no trace of testicular development in either side.

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Grants

  1. AI-19456/NIAID NIH HHS
  2. CA-08748/NCI NIH HHS
  3. HD-00171/NICHD NIH HHS

MeSH Term

Adolescent
Female
Gonadal Dysgenesis
Gonadal Dysgenesis, 46,XY
H-Y Antigen
HLA Antigens
Humans
Lymphocytes
Ovary
Phenotype

Chemicals

H-Y Antigen
HLA Antigens

Word Cloud

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