MUCOLIPIDOSIS TYPE-IV - CLINICAL MANIFESTATIONS AND NATURAL-HISTORY

被引:49
作者
CHITAYAT, D
MEUNIER, CM
HODGKINSON, KA
SILVER, K
FLANDERS, M
ANDERSON, IJ
LITTLE, JM
WHITEMAN, DAH
CARPENTER, S
机构
[1] MONTREAL CHILDRENS HOSP,DEPT PEDIAT,DIV NEUROL,MONTREAL H3H 1P3,QUEBEC,CANADA
[2] MONTREAL CHILDRENS HOSP,DEPT PEDIAT,DIV OPHTHALMOL,MONTREAL H3H 1P3,QUEBEC,CANADA
[3] MONTREAL NEUROL HOSP & INST,DEPT NEUROL NEUROSURG & PATHOL,MONTREAL H3A 2B4,QUEBEC,CANADA
[4] MCGILL UNIV,MONTREAL H3A 2T5,QUEBEC,CANADA
[5] UNIV CONNECTICUT,SCH MED,DEPT PEDIAT,FARMINGTON,CT 06032
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1991年 / 41卷 / 03期
关键词
LYSOSOMAL STORAGE; ELECTRON MICROSCOPY; SKIN BIOPSY; CONJUNCTIVAL BIOPSY; CORNEAL CLOUDINESS; DEVELOPMENTAL DELAY; ASHKENAZI-JEWISH; PIGMENTARY RETINOPATHY; AUTOSOMAL RECESSIVE INHERITANCE;
D O I
10.1002/ajmg.1320410310
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The clinical manifestations and psychomotor development of five patients with mucolipidosis IV (MLIV) from three Ashkenazi-Jewish families are reported. The presenting symptoms were hypotonia, developmental delay, corneal clouding, and puffy eyelids. Four of the patients had convergent strabismus and none progressed beyond a developmental age of 15 months. One patient died of aspiration at 17 years while the oldest patient entered puberty at 20 years, developed a coarse face at 30 years, and is now 32 years old. Histopathological studies in four patients showed storage changes characteristic of MLIV.
引用
收藏
页码:313 / 318
页数:6
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