Rare Disease: Alström Syndrome

May 17, 2018
Alström syndrome is a rare inherited autosomal recessive syndrome characterized by the onset of obesity in childhood or adolescence, Type 2 diabetes with severe insulin resistance, dyslipidemia, hypertension and severe multi-organ fibrosis, involving the liver, kidney and heart. Alström syndrome is also characterized by a progressive loss of vision and hearing, a form of heart disease that enlarges and weakens the heart muscle (dilated cardiomyopathy), and short stature. This disorder can also cause serious or life-threatening medical problems involving the liver, kidneys, bladder, and lungs. Some individuals with Alström syndrome have a skin condition called acanthosis nigricans, which causes the skin in body folds and creases to become thick, dark, and velvety. The signs and symptoms of Alström syndrome vary in severity, and not all affected individuals have all of the characteristic features of the disorder. Prometic has shown early efficacy results with a promising drug candidate -PBI-4050. PBI-4050 is an investigational drug currently being tested in an open label clinical trial in the UK and not approved for sale.

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Alstrom Syndrome 'Living with a Rare Disease'
Alstrom Syndrome 'Living with a Rare Disease'

Raising awareness and understanding about this ultra rare condition. Strength for today, hope for the future