ANGIOKERATOMA CORPORIS DIFFUSUM IN A PATIENT WITH NORMAL ENZYME-ACTIVITIES

被引:35
作者
HOLMES, RC
FENSOM, AH
MCKEE, P
CAIRNS, RJ
BLACK, MM
机构
[1] ST THOMAS HOSP,DEPT PATHOL,LONDON SE1 7EH,ENGLAND
[2] GUYS HOSP,PAEDIAT RES UNIT,LONDON SE1 9RT,ENGLAND
[3] ST BARTHOLOMEWS HOSP,LONDON EC1A 7BE,ENGLAND
关键词
D O I
10.1016/S0190-9622(84)80012-2
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:384 / 387
页数:4
相关论文
共 11 条
[1]  
EPINETTE WW, 1973, ARCH DERMATOL, V107, P754
[2]  
GATTI R, 1973, LANCET, V2, P1024
[3]  
KOUSSEFF BG, 1973, LANCET, V2, P1387
[4]  
LOONEN MCB, 1974, LANCET, V2, P785
[5]  
LOWDEN JA, 1979, AM J HUM GENET, V31, P1
[6]   ANGIOKERATOMA CORPORIS DIFFUSUM WITH FEATURES OF A MUCOPOLYSACCHARIDOSIS [J].
MCCALLUM, DI ;
MACADAM, RF ;
JOHNSTON, AW .
JOURNAL OF MEDICAL GENETICS, 1980, 17 (01) :21-26
[7]   ADULT TYPE NEURONAL STORAGE DISEASE WITH NEURAMINIDASE DEFICIENCY [J].
MIYATAKE, T ;
ATSUMI, T ;
OBAYASHI, T ;
MIZUNO, Y ;
ANDO, S ;
ARIGA, T ;
MATSUINAKAMURA, K ;
YAMADA, T .
ANNALS OF NEUROLOGY, 1979, 6 (03) :232-244
[8]   DEFICIENCY OF ALPHA-L-FUCOSIDASE [J].
PATEL, V ;
WATANABE, I ;
ZEMAN, W .
SCIENCE, 1972, 176 (4033) :426-&
[9]  
PELTIER A, 1977, BIOMEDICINE, V26, P194
[10]  
PRIMROSE DA, 1975, J MENT DEFIC RES, V19, P267