X-LINKED DOMINANT CONRADI-HUNERMANN SYNDROME PRESENTING AS CONGENITAL ERYTHRODERMA

被引:40
作者
KALTER, DC
ATHERTON, DJ
CLAYTON, PT
机构
[1] ST JOHNS HOSP DIS SKIN,LONDON WC2H 7BJ,ENGLAND
[2] HOSP SICK CHILDREN,LONDON WC1N 3JH,ENGLAND
[3] INST CHILD HLTH,LONDON WC1N 1EH,ENGLAND
关键词
D O I
10.1016/S0190-9622(89)70169-9
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
引用
收藏
页码:248 / 256
页数:9
相关论文
共 41 条
[1]  
BADOIS C, 1983, ANN RADIOL, V26, P244
[2]  
BERGSTROM K, 1972, CLIN GENET, V3, P158
[3]   DIHYDROXYACETONE PHOSPHATE ACYLTRANSFERASE DEFICIENCY IN PEROXISOMAL DISORDERS [J].
BESLEY, GTN ;
BROADHEAD, DM .
JOURNAL OF INHERITED METABOLIC DISEASE, 1987, 10 :236-238
[5]  
BURCK V, 1982, EUR J PEDIATR, V138, P67
[6]   PLASMA BILE-ACIDS IN PATIENTS WITH PEROXISOMAL DYSFUNCTION SYNDROMES - ANALYSIS BY CAPILLARY GAS-CHROMATOGRAPHY MASS-SPECTROMETRY [J].
CLAYTON, PT ;
LAKE, BD ;
HALL, NA ;
SHORTLAND, DB ;
CARRUTHERS, RA ;
LAWSON, AM .
EUROPEAN JOURNAL OF PEDIATRICS, 1987, 146 (02) :166-173
[7]  
COLLINS P, 1977, AM J OBSTET GYNECOL, V127, P444
[8]  
Conradi, 1914, JB KINDERHEILK, V80, P86
[9]   ACUTE SKIN MANIFESTATIONS OF CONRADI-HUENERMANN SYNDROME IN A MALE-ADULT [J].
CROVATO, F ;
REBORA, A .
ARCHIVES OF DERMATOLOGY, 1985, 121 (08) :1064-1065
[10]   INHERITED CHONDRODYSPLASIA PUNCTATA DUE TO A DELETION OF THE TERMINAL SHORT ARM OF AN X-CHROMOSOME [J].
CURRY, CJR ;
MAGENIS, RE ;
BROWN, M ;
LANMAN, JT ;
TSAI, J ;
OLAGUE, P ;
GOODFELLOW, P ;
MOHANDAS, T ;
BERGNER, EA ;
SHAPIRO, LJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 311 (16) :1010-1015