HALLERMANN-STREIFF SYNDROME - A REVIEW

被引:62
作者
COHEN, MM
机构
[1] DALHOUSIE UNIV,FAC DENT,DEPT PEDIAT,HALIFAX B3H 3J5,NS,CANADA
[2] DALHOUSIE UNIV,FAC MED,HALIFAX B3H 3J5,NS,CANADA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1991年 / 41卷 / 04期
关键词
HALLERMANN-STREIFF SYNDROME;
D O I
10.1002/ajmg.1320410423
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Hallermann-Streiff syndrome is characterized by dyscephaly, hypotrichosis, microphthalmia, cataracts, beaked nose, micrognathia, and proportionate short stature. Cause is unknown; sporadic occurrence is the rule. Data presented in this review include the characteristics of pregnancy, growth and development, principal manifestations, radiographic and ophthalmological characteristics, and the results of cephalometric study. Potential complications in the syndrome are related to the narrow upper airway associated with the craniofacial configuration. Severe complications may include early pulmonary infection, respiratory embarrassment, obstructive sleep apnea, and anesthetic risk. Topics for future study are suggested.
引用
收藏
页码:488 / 499
页数:12
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