PROTEUS SYNDROME - CLINICAL-EVIDENCE FOR SOMATIC MOSAICISM AND SELECTIVE REVIEW

被引:105
作者
COHEN, MM [1 ]
机构
[1] DALHOUSIE UNIV,FAC MED,DEPT PEDIAT,HALIFAX B3H 3J5,NS,CANADA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 47卷 / 05期
关键词
ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; CONNECTIVE TISSUE NEVUS; UNCOMMON NEOPLASMS; PULMONARY ABNORMALITIES; RENAL ABNORMALITIES; BRAIN MALFORMATIONS; SEVERE MENTAL DEFICIENCY; SEIZURES; FACIAL PHENOTYPE; ABNORMAL CRANIOFACIAL GROWTH;
D O I
10.1002/ajmg.1320470514
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
I report 2 unusual cases of Proteus syndrome that support the concept of somatic mosaicism. In one patient, a huge connective tissue nevus covered the chest and abdomen and hyperostoses of the calvaria were observed. In the other patient, linear verrucous epidermal nevi, epibulbar dermoids, and hyperostoses were found. No enlargement of the limbs or digits occurred and the plantar surfaces of the feet were normal. Selective aspects of Proteus syndrome not previously reviewed are also presented including: uncommon neoplasms; pulmonary and renal abnormalities; brain malformations; facial phenotype associated with seizures and severe mental deficiency; and types of abnormal growth in the craniofacial skeleton. (C) 1993 Wiley-Liss, Inc.
引用
收藏
页码:645 / 652
页数:8
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