Simultaneous occurrence of neurofibromatosis type 1 and tuberous sclerosis in a young girl

被引:9
作者
Wheeler, PG
Sadeghi-Nejad, A
机构
[1] Nemours Childrens Clin, Div Genet & Metab, Orlando, FL 32806 USA
[2] Tufts Univ, Sch Med, Dept Pediat, Div Endocrinol, Boston, MA 02111 USA
[3] Tufts Univ New England Med Ctr, Floating Hosp Children, Boston, MA 02111 USA
关键词
neurofibromatosis type 1; tuberous sclerosis complex; neurocutaneous disorders;
D O I
10.1002/ajmg.a.30530
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Neurofibromatosis type 1 and tuberous sclerosis are the two most common neurocutaneous disorders in humans. Both are transmitted as autosomal dominant conditions with a high rate of new mutations and similar clinical features. However, the two disorders have distinct and well-delineated genetic, biochemical, and physical findings. Simultaneous occurrence of these two conditions is rare. We report on a young girl who inherited both disorders, review similar cases reported in the world literature, and discuss possible implications of the presence of NF1 and TSC in the same individual. (C) 2005 Wiley-Liss, Inc.
引用
收藏
页码:78 / 81
页数:4
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