Results 141 to 150 of about 5,328,161 (151)
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[Type II Leydig cell hypoplasia caused by LHCGR gene mutation: a case report].
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatricsThe patient, assigned female at birth and aged 1 year and 7 months, presented with clinical manifestations of 46,XY disorders of sex development. The external genitalia exhibited a severely undermasculinized phenotype. Laboratory tests and gonadal biopsy indicated poor Leydig cell function and good Sertoli cell function.
Ke-Xin, Jin +6 more
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A Novel Variant in LCHGR Gene in 3 Siblings With Type 1 Leydig Cell Hypoplasia
Gynecological Endocrinology, 2020Amine Aktar Karakaya +2 more
exaly
[Leydig cell hypoplasia (Leydig cell aplasia)].
Nihon rinsho. Japanese journal of clinical medicine, 2006Osamu, Arisaka, Satomi, Koyama
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Leydig cell hypoplasia determining familial hypergonadotropic hypogonadism.
Progress in clinical and biological research, 1986S P, Toledo +4 more
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Mutations in a novel primate-specific cryptic exon of the LHCGR gene cause Leydig cell hypoplasia
Experimental and Clinical Endocrinology & Diabetes, 2007N Kossack +3 more
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Leydig Cell Hypoplasia in Three Siblings in the Same Family
2019ÖZDEN, AYŞE +2 more
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Laparoscopic bilateral gonadectomy in a phenotypic female with a form of leydig cell hypoplasia
The Journal of the American Association of Gynecologic Laparoscopists, 1995openaire +1 more source
[Congenital Leydig cell hypoplasia and aplasia].
Ryoikibetsu shokogun shirizu, 1995openaire +1 more source