HYDROLETHALUS SYNDROME IN CONSECUTIVE AFRICAN SIBLINGS

被引:15
作者
ADETORO, OO
KOMOLAFE, F
ANJORIN, A
机构
[1] UNIV ILORIN, DEPT RADIOL, ILORIN, NIGERIA
[2] UNIV ILORIN, DEPT OBSTET & GYNECOL, ILORIN, NIGERIA
[3] UNIV ILORIN, DEPT PATHOL, ILORIN, NIGERIA
关键词
D O I
10.1007/BF02343433
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Hydrolethalus syndrome may comprise mainly hydrocephalus, polydactyly, micrognathia, congenital cardiac and respiratory anomalies and uniform lethality. It was recently described in Finland, with a suggestion that it might be one of the Finnish diseases. Two [human infant] cases of this syndrome in consecutive siblings of a Nigerian couple are reported on. In addition, associated healing fractures of the long bones are described, a feature not mentioned in the original report, apparently because those cases were not subjected to post-partum radiography.
引用
收藏
页码:422 / 424
页数:3
相关论文
共 4 条
[1]  
BARK M, 1979, MED IMAGING, P191
[2]  
FRASER FC, 1957, J CHRON DIS, V10, P97
[3]  
OPITZ J M, 1969, Birth Defects Original Article Series, V5, P167
[4]  
SALONEN R, 1981, CLIN GENET, V19, P321