18P- SYNDROME AND HYPOPITUITARISM

被引：25

作者：

ARTMAN, HG ^{[1
]}

MORRIS, CA ^{[1
]}

STOCK, AD ^{[1
]}

机构：

[1] UNIV NEVADA,SCH MED,DEPT PATHOL,RENO,NV 89557

来源：

JOURNAL OF MEDICAL GENETICS | 1992年 / 29卷 / 09期

关键词：

D O I：

10.1136/jmg.29.9.671

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

A patient is described with 18p- syndrome and hypopituitarism. This is the first patient with this syndrome who has been shown to benefit from growth hormone therapy. Patients with this syndrome who have growth deficiency should be considered for evaluation for hypopituitarism, if the quality of their lives would improve with an increase in stature.

引用

页码：671 / 672

页数：2

共 7 条

[1] GROWTH-HORMONE, SUSPECTED GONADOTROPIN-DEFICIENCY, AND RING-18 CHROMOSOME [J].