Alstrom syndrome (OMIM 203800): a case report and literature review

被引:0
作者
Tisha Joy
Henian Cao
Graeme Black
Rayaz Malik
Valentine Charlton-Menys
Robert A Hegele
Paul N Durrington
机构
[1] University of Western Ontario,Department of Vascular Biology and Medicine, Robarts Research Institute and Schulich School of Medicine and Dentistry
[2] Medical Genetics,Clinical and Laboratory Sciences
[3] Eye Hospital,undefined
[4] Cardiovascular Research Group,undefined
[5] School of Clinical & Laboratory Sciences,undefined
来源
Orphanet Journal of Rare Diseases | / 2卷
关键词
Sensorineural Hearing Loss; Young Sister; Acanthosis Nigricans; Sensorineural Deafness; H3882Y Mutation;
D O I
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[1]  
Alstrom CH(1959)Retinal degeneration combined with obesity, diabetes mellitus and neurogenous deafness: a specific syndrome (not hitherto described) distinct from the Laurence-Moon-Bardet-Biedl syndrome: a clinical, endocrinological and genetic examination based on a large pedigree Acta psychiatrica et neurologica Scandinavica 129 1-35
[2]  
Hallgren B(2006)Syndromic obesity and diabetes: changes in body composition with age and mutation analysis of ALMS1 in 12 United Kingdom kindreds with Alstrom syndrome The Journal of clinical endocrinology and metabolism 91 3110-3116
[3]  
Nilsson LB(2005)New Alstrom syndrome phenotypes based on the evaluation of 182 cases Archives of internal medicine 165 675-683
[4]  
Asander H(1997)Genealogy, natural history, and phenotype of Alstrom syndrome in a large Acadian kindred and three additional families American journal of medical genetics 73 150-161
[5]  
Minton JA(2004)Hypertriglyceridaemia in Alstrom's syndrome: causes and associations in 37 cases Clinical endocrinology 60 228-231
[6]  
Owen KR(2002)Evaluation of insulin resistant diabetes mellitus in Alstrom syndrome: a long-term prospective follow-up of three siblings Diabetes research and clinical practice 56 189-196
[7]  
Ricketts CJ(2002)Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alstrom syndrome Nature genetics 31 79-83
[8]  
Crabtree N(2002)Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alstrom syndrome Nature genetics 31 74-78
[9]  
Shaikh G(2005)Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes Diabetes 54 1581-1587
[10]  
Ehtisham S(2007)A role for Alstrom syndrome protein, alms1, in kidney ciliogenesis and cellular quiescence PLoS genetics 3 e8-984