CUTIS MARMORATA TELANGIECTATICA CONGENITA

被引:21
作者
KENNEDY, C
ORANJE, AP
KEIZER, K
VANDENHEUVEL, MM
CATSMANBERREVOETS, CE
机构
[1] ERASMUS UNIV,HOSP DIJKZIGT,DEPT NEUROL,3015 GD ROTTERDAM,NETHERLANDS
[2] ERASMUS UNIV,HOSP DIJKZIGT,DEPT PEDIAT,3015 GD ROTTERDAM,NETHERLANDS
[3] SOPHIA CHILDRENS UNIV HOSP,ROTTERDAM,NETHERLANDS
关键词
D O I
10.1111/j.1365-4362.1992.tb03564.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The authors describe ten cases of cutis marmorata telangiectatica congenita (CMTC). All of these cases were sporadic. The incidence of associated anomalies was relatively low, and three patients had skin manifestations (cutaneous atrophy and nevus telangiectaticus). In two patients, the right leg was shorter and thinner. Another two showed neurologic symptoms without lasting neurologic damage. New associated anomalies, such as tendinitis stenosans and bowing of the lower legs, did not provide additional information regarding the cause of CMTC. The authors suggest that Happle's lethal gene hypothesis for Klippel-Trenaunay and Sturge-Weber syndromes also could be applied to CMTC.
引用
收藏
页码:249 / 252
页数:4
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