The role of Y chromosome deletions in male infertility
Author(s) -
Keyi Ma,
Con Mallidis,
Shalender Bhasin
Publication year - 2000
Publication title -
european journal of endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.897
H-Index - 148
eISSN - 1479-683X
pISSN - 0804-4643
DOI - 10.1530/eje.0.1420418
Subject(s) - azoospermia , infertility , male infertility , y chromosome , spermatogenesis , biology , andrology , azoospermia factor , y chromosome microdeletion , chromosome , genetics , gene , long arm , medicine , endocrinology , pregnancy
Male infertility affects approximately 2-7% of couples around the world. Over one in ten men who seek help at infertility clinics are diagnosed as severely oligospermic or azoospermic. Recent extensive molecular studies have revealed that deletions in the azoospermia factor region of the long arm of the Y chromosome are associated with severe spermatogenic impairment (absent or severely reduced germ cell development). Genetic research into male infertility, in the last 7 years, has resulted in the isolation of a great number of genes or gene families on the Y chromosome, some of which are believed to influence spermatogenesis.
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