CLEFT-LIP AND PALATE, SENSORINEURAL DEAFNESS, AND SACRAL LIPOMA IN 2 BROTHERS - A POSSIBLE EXAMPLE OF THE DISORGANIZATION MUTANT

被引:23
作者
LOWRY, RB
YONG, SL
机构
[1] ALBERTA CHILDRENS PROV GEN HOSP,RES CTR,CALGARY T2T 5C7,ALBERTA,CANADA
[2] UNIV BRITISH COLUMBIA,UNIV HOSP,DEPT MED GENET,VANCOUVER V6T 1W5,BC,CANADA
关键词
D O I
10.1136/jmg.28.2.135
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report two brothers of Chinese origin who have an apparently unique syndrome of cleft lip/palate, profound sensorineural deafness, and a sacral lipoma. Additional findings which were not common to both were aberrant digital appendages on the heel and thigh of one boy and an anterior sacral meningocele and dislocated hip in the other. Intelligence is normal in both. Both boys suffer from functional constipation but biopsy studies showed no evidence of Hirschsprung's disease. The parents, who are normal, are not related. Inheritance is probably autosomal or X linked recessive. A possible link with the disorganisation mouse mutant is discussed.
引用
收藏
页码:135 / 137
页数:3
相关论文
共 4 条
[1]  
COHEN MM, 1978, CLEFT PALATE J, V15, P306
[2]  
HUMMEL KP, 1959, PEDIATRICS, V23, P212
[3]  
LYON MF, 1989, GENETIC VARIANTS STR, P92
[4]   A POSSIBLE HUMAN HOMOLOG FOR THE MOUSE MUTANT DISORGANIZATION [J].
WINTER, RM ;
DONNAI, D .
JOURNAL OF MEDICAL GENETICS, 1989, 26 (07) :417-420