Natural history of Alstrom syndrome in early childhood: Onset with dilated cardiomyopathy

被引:76
作者
Michaud, JL
Heon, E
Guilbert, F
Weill, J
Puech, B
Benson, L
Smallhorn, JF
Shuman, CT
Buncic, JR
Levin, AV
Weksberg, R
Breviere, GM
机构
[1] HOSP SICK CHILDREN, DEPT GENET, DIV CLIN GENET, TORONTO, ON M5G 1X8, CANADA
[2] HOSP SICK CHILDREN, DEPT OPHTHALMOL, TORONTO, ON M5G 1X8, CANADA
[3] HOSP SICK CHILDREN, DEPT PEDIAT, DIV CARDIOL, TORONTO, ON M5G 1X8, CANADA
[4] CTR HOSP REG UNIV LILLE, SERV OPHTALMOL, PEDIAT ENDOCRINE UNIT, LILLE, FRANCE
[5] CTR HOSP REG UNIV LILLE, SERV OPHTALMOL, SERV CARDIOL INFANTILE, LILLE, FRANCE
关键词
D O I
10.1016/S0022-3476(96)70394-3
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Alstrom syndrome is an autosomal recessive disorder characterized by cone-rod dystrophy, obesity, hearing impairment, and diabetes caused by insulin resistance. By reviewing the charts of eight patients followed for periods of 2 to 22 years, we established the natural history of this syndrome during childhood. Five patients, in four families, were seen between the ages of 3 weeks and 4 months with a dilated cardiomyopathy, a previously unrecognized feature of the syndrome. Photophobia and nystagmus were first documented in the eight patients between the ages of 5 months and 15 months. In all patients, electroretinography initially showed a severe cone impairment with mild (2/8) or no (6/8) rod involvement. Electroretinograms, obtained again at ages 9 to 22 years for four patients, revealed extinguished rod-and-cone responses, Obesity developed during childhood in seven patients, in at least three of them before age 2 years. Hearing impairment (5/8) and diabetes/glucose intolerance (4/8) were diagnosed at the end of the first decade or during the second decade. This constellation of features should facilitate early diagnosis of the syndrome.
引用
收藏
页码:225 / 229
页数:5
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