A SYNDROME OF CONGENITAL HYPOPLASIA OF THE ALAE NASI, SITUS INVERSUS, AND SEVERE HYPOPROTEINEMIA IN 2 SIBLINGS

被引:21
作者
HELIN, I [1 ]
JODAL, U [1 ]
机构
[1] GOTHENBURG UNIV, OSTRA SJUKHUSET, S-41124 GOTHENBURG, SWEDEN
关键词
D O I
10.1016/S0022-3476(81)80026-1
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:932 / 934
页数:3
相关论文
共 6 条
[1]   FOCAL DERMAL HYPOPLASIA SYNDROME . A REVIEW OF LITERATURE AND REPORT OF 2 CASES [J].
GOLTZ, RW ;
HENDERSO.RR ;
HITCH, JM ;
OTT, JE .
ARCHIVES OF DERMATOLOGY, 1970, 101 (01) :1-&
[2]   SYNDROME OF CONGENITAL APLASIA OF ALAE NASI, DEAFNESS, HYPOTHYROIDISM, DWARFISM, ABSENT PERMANENT TEETH, AND MALABSORPTION [J].
JOHANSON, A ;
BLIZZARD, R .
JOURNAL OF PEDIATRICS, 1971, 79 (06) :982-+
[3]   TRYPSINOGEN DEFICIENCY DISEASE [J].
MORRIS, MD ;
FISHER, DA .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1967, 114 (02) :203-&
[4]   OCULODENTODIGITAL DYSPLASIA [J].
REISNER, SH ;
KOTT, E ;
BORNSTEIN, B ;
SALINGER, H ;
KAPLAN, I ;
GORLIN, RJ .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1969, 118 (04) :600-+
[5]  
STUPKA W, 1938, MISSBILDUNGEN ANOMAL
[6]  
TOWNES P L, 1972, Birth Defects Original Article Series, V8, P95