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Arch Ophthalmol ; 107(6): 855-7, 1989 Jun.
Article in English | MEDLINE | ID: mdl-2730406

ABSTRACT

We studied a family with the Bardet-Biedl syndrome and diabetes mellitus. Two affected brothers and one affected sister were examined. Two older sisters with stigmata of the syndrome had died of unclear causes. The 18-year-old brother was obese, was mentally retarded, and had pigmentary retinopathy and insulin-dependent diabetes mellitus. The 16-year-old sister, who died in a diabetic coma during the course of the investigation, had polydactyly, hypogenitalism, obesity, mental retardation, and pigmentary retinopathy. The 8-year-old brother had all the features of the syndrome, but no overt diabetes mellitus. Electroretinography showed severe cone and rod dysfunction. Patients with the Bardet-Biedl syndrome should be screened for the presence of abnormalities in glucose metabolism.


Subject(s)
Diabetes Mellitus, Type 1/genetics , Intellectual Disability/genetics , Obesity/genetics , Retinitis Pigmentosa/genetics , Adolescent , Child , Diabetes Mellitus, Type 1/diagnosis , Diagnosis, Differential , Electroretinography , Family , Female , Humans , Intellectual Disability/diagnosis , Laurence-Moon Syndrome/diagnosis , Male , Obesity/diagnosis , Pedigree , Photoreceptor Cells/physiopathology , Prader-Willi Syndrome/diagnosis , Retinitis Pigmentosa/diagnosis , Syndrome
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