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Medicine (Baltimore) ; 96(10): e6192, 2017 Mar.
Article in English | MEDLINE | ID: mdl-28272210

ABSTRACT

RATIONALE: Alström syndrome is an autosomal recessive disorder characterized by hearing loss, blindness, obesity, non-insulin dependent diabetes, and others. PATIENT CONCERN: A 10 years old Saudi girl, who presented with diabetic ketoacidosis and found to have hearing loss and blindness. DIAGNOSIS: Alström syndrome. INTERVENTIONS: Multidisciplinary team approach, with echocardiography, hearing test, eye exam and genetic test for Alström syndrome. OUTCOMES: The patient has retinitis pigmentosa, bilateral hearing loss, double diabetes with weakly positive anti-insulin antibodies and DNA analysis showed novel mutation for Alström syndrome. LESSONS: the combination of obesity, diabetes, hearing loss and blindness should alert the physician to test for Alström syndrome.


Subject(s)
Alstrom Syndrome/genetics , Proteins/genetics , Cell Cycle Proteins , Child , DNA Mutational Analysis , Diabetes Mellitus/etiology , Female , Humans
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