Category:Beals syndrome

**Congenital contractural arachnodactyly**
	human disease
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Instance of	rare disease; class of disease;
Subclass of	primary bone dysplasia; distal arthrogryposis; autosomal dominant disease;
Authority file
	Q3508618;
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Beals syndrome is caused by a mutation in a gene that helps build connective tissue called fibrillin-2. It is closely related to the gene (fibrillin-1) that causes Marfan syndrome. Beals syndrome is also known as congenital contractural arachnoldactyly (CCA), which refers to the joint contractures (shortening) that are key features of the syndrome.

Media in category "Beals syndrome"

The following 2 files are in this category, out of 2 total.

אוזן תסמונת בילס.jpg 1,200 × 1,600; 179 KB
יד תסמונת בילס.jpg 1,600 × 1,386; 269 KB

Category:Beals syndrome

Media in category "Beals syndrome"

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