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Mixed testicular dysgenesis and 46, XY/47, XXY mosaicism
Author(s) -
Frajese G.,
Santiemma V.,
Savioli M.,
Fraccaro M.
Publication year - 1973
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1973.tb01133.x
Subject(s) - azoospermia , dysgenesis , medicine , endocrinology , germinal epithelium , gonadal dysgenesis , testosterone (patch) , biology , andrology , histology , anatomy , spermatogenesis , pregnancy , genetics , infertility
A 20‐year‐old 46, XY/47, XXY mosaic with azoospermia, testicular hypotrophy, low testosterone and high gonadotrophin levels had a mixed testicular dysgenesis. Histology revealed alternating tubules with germinal aplasia and tubules with spermatidic arrest.

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