STUDIES OF MALFORMATION SYNDROMES OF MAN .50. JOHANSON-BLIZZARD SYNDROME - CASE-REPORT AND AUTOPSY FINDINGS

被引:45
作者
DAENTL, DL
FRIAS, JL
GILBERT, EF
OPITZ, JM
机构
[1] UNIV WISCONSIN,CTR HLTH SCI,DEPT PATHOL,MADISON,WI 53706
[2] UNIV WISCONSIN,CTR HLTH SCI,DEPT PEDIAT,MADISON,WI 53706
[3] WISCONSIN CLIN GENET CTR,MADISON,WI
[4] UNIV FLORIDA,DEPT PEDIAT,GAINESVILLE,FL 32611
[5] UNIV CALIF SAN FRANCISCO,DEPT PEDIAT,SAN FRANCISCO,CA 94143
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1979年 / 3卷 / 02期
关键词
D O I
10.1002/ajmg.1320030203
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The authors report a case of a boy with the Johanson-Blizzard syndrome who died at the age of 8 years with complications of pancreatic exocrine insufficiency, and at autopsy was found to have a small thyroid filled with colloid, virtually complete replacement of the pancreas with adipose tissue, and a brain of normal size but with evidence of a cortical developmental defect consisting of abnormalities of gyral formation and of cortical neuronal organization. In addition the boy had postnatal growth failure, apparent severe mental retardation, congenital scalp defects and scalp hair patterning abnormalities, aplasia of the nasal alae, nasolacrimo-cutaneous fistulae, hypotonia, severe congenital sensorineural deafness, and small conical and widely spaced teeth. Evidence is accumulating that this syndrome is likely to be inherited as an autosomal recessive disorder. This case represents the first report of autopsy findings in the syndrome.
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收藏
页码:129 / 135
页数:7
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