Hypertriglyceridaemia in Alström's syndrome: causes and associations in 37 cases
✍ Scribed by R. B. Paisey; C. M. Carey; L. Bower; J. Marshall; P. Taylor; P. Maffei; P. Mansell
- Book ID
- 108702877
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 176 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0300-0664
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Alström syndrome is an autosomal recessive disorder (MIM No. \*203800) characterized by retinal degeneration, obesity, deafness, noninsulin-dependent diabetes mellitus, and nephropathy. We report two sibs with Alström syndrome and hepatic dysfunction. The first sib developed elevations in liver enzy
Alström syndrome is a monogenic recessive disorder featuring an array of clinical manifestations, with systemic fibrosis and multiple organ involvement, including retinal degeneration, hearing loss, childhood obesity, diabetes mellitus, dilated cardiomyopathy (DCM), urological dysfunction, and pulmo