CROUZON SYNDROME WITH SHORT STATURE - CASE-REPORT

被引：3
|
作者：
FEILD, CR
LEIBER, A
TONIGES, C
机构：
[1] USA HOSP, EXCEPT FAMILY MEMBER SERV, WURZBURG, GERMANY
[2] UNIV WURZBURG, W-8700 WURZBURG, GERMANY
来源：
AMERICAN JOURNAL OF THE MEDICAL SCIENCES | 1991年 / 302卷 / 02期
关键词：
CRANIOSYNOSTOSIS; CROUZON SYNDROME; GROWTH HORMONE DEFICIENCY; SHORT STATURE;
D O I：
10.1097/00000441-199108000-00006
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
A five-year-old boy with Crouzon Syndrome, short stature, and delayed bone age was found to have partial growth hormone deficiency. Accelerated growth was observed after human growth hormone replacement. Children with Crouzon Syndrome should be followed closely for all growth parameters, not just head circumference.
引用
收藏
页码：101 / 102
页数：2
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