X-LINKED HYPOGONADISM, GYNECOMASTIA, MENTAL-RETARDATION, SHORT STATURE, AND OBESITY - NEW SYNDROME

被引：50

作者：

VASQUEZ, SB ^{[1
]}

HURST, DL ^{[1
]}

SOTOS, JF ^{[1
]}

机构：

[1] OHIO STATE UNIV, COLL MED, DEPT PEDIAT, DIV ENDOCRINOL & METAB, COLUMBUS, OH 43210 USA

来源：

JOURNAL OF PEDIATRICS | 1979年 / 94卷 / 01期

关键词：

D O I：

10.1016/S0022-3476(79)80350-9

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Five male members in four generations of the same family had hypogonadism, gynecomastia, mentalretardation, obesity, and short stature. The X-linked mode of inheritance, the distinctive facies, the normal size of the hands and feet, and the true gynecomastia are the main characteristics. Endocrine evaluation and histologic studies of the testes suggest partial hypogonadotropic hypogonadism. This disorder represents a new syndrome distinct from others previously described. © 1979 The C. V. Mosby Company.

引用

页码：56 / 60

页数：5

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