Combined Leydig cell and Sertoli cell dysfunction in 46,XX males lacking the sex determining region Y gene.
Combined Leydig cell and Sertoli cell dysfunction in 46,XX males lacking the sex determining region Y gene.
复制标题
缺乏性别决定区 Y 基因的 46,XX 男性的间质细胞和支持细胞功能障碍。
DOI:
10.1002/ajmg.1320570315
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发表时间:
1995
期刊:
影响因子:
--
通讯作者:
Berkovitz,GD
中科院分区:
文献类型:
--
作者:
Turner,B;Fechner,PY;Fuqua,JS;Marcantonio,SM;Perlman,EJ;Vordermark,JS;Berkovitz,GD
We have evaluated 3 individuals with a rare form of 46, XX sex reversal. All of them had ambiguous external genitalia and mixed wolffian and mullerian structures, indicating both Leydig cell and Sertoli cell dysfunction, similar to that of patients with true hermaphroditism. However, gonadal tissue was not ovotesticular but testicular with varying degrees of dysgenesis.SRY sequences were absent in genomic DNA from peripheral leukocytes in all 3 subjects. Y centromere sequences were also absent, indicating that testis development did not occur because of a low level mosaicism of Y bearing cells. The subjects in this report demonstrate that there is a continuum in the extent of testis determination in SRY‐negative 46, XX sex reversal, ranging from nearly normal to minimal testicular development. © 1995 Wiley‐Liss, Inc.
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DOI:
10.1016/0140-6736(90)93270-y
发表时间:
1990
期刊:
The Lancet
影响因子:
--
作者:
M. Ferguson;M. North;N. Affara;H. Briggs
通讯作者:
H. Briggs
DOI:
10.1073/pnas.90.8.3368
发表时间:
1993-04-15
影响因子:
11.1
作者:
MCELREAVEY, K;VILAIN, E;FELLOUS, M
通讯作者:
FELLOUS, M
影响因子:
168.9
作者:
M. Ferguson
通讯作者:
M. Ferguson
DOI:
10.1016/s0022-3476(75)80068-0
发表时间:
1975
期刊:
The Journal of pediatrics
影响因子:
--
作者:
S. Duck;G. Sekhon;R. Wilbois;A. Pagliara;V. Weldon
通讯作者:
V. Weldon
DOI:
10.1016/s0022-3476(87)80162-2
发表时间:
1987
期刊:
The Journal of pediatrics
影响因子:
--
作者:
N. Skordis;D. Stetka;M. Macgillivray;S. Greenfield
通讯作者:
S. Greenfield