HYPOTHALAMIC HAMARTOMA IN ORAL-FACIAL-DIGITAL SYNDROME TYPE-VI (VARADI-SYNDROME)

被引:28
作者
STEPHAN, MJ [1 ]
BROOKS, KL [1 ]
MOORE, DC [1 ]
COLL, EJ [1 ]
GOHO, C [1 ]
机构
[1] MADIGAN ARMY MED CTR, DEPT PEDIAT DENT, TACOMA, WA 98431 USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1994年 / 51卷 / 02期
关键词
HYPOTHALAMIC HAMARTOMA; CEREBELLAR VERMIS HYPOPLASIA; DANDY-WALKER MALFORMATION; SUPERNUMERARY INCISOR; MESIODENS; POLYDACTYLY; SYNDACTYLY; PRECOCIOUS PUBERTY;
D O I
10.1002/ajmg.1320510209
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Oral-facial-digital syndrome (OFDS) type VI (Varadi syndrome) is an autosomal recessive trait of orofacial anomalies, cerebellar dysgenesis, and polysyndactyly. Developmental anomalies of the posterior fossa, including cerebellar hypoplasia and variants of the Dandy-Walker complex, are the most common central nervous system malformations reported in patients with this syndrome. We report hypothalamic hamartoma, supernumerary maxillary incisor, and precocious puberty in a boy with OFDS type VI. We propose that hypothalamic hamartoma is an occasional manifestation of OFDS type VI. (C) 1994 Wiley-Liss, Inc.
引用
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页码:131 / 136
页数:6
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