Beals syndrome is caused by a mutation in a gene that helps build connective tissue called fibrillin-2. Beals syndrome is also known as congenital contractural arachnoldactyly CCA , which refers to the joint contractures shortening that are key features of the syndrome..Beals syndrome is an extremely rare genetic disorder characterized by the permanent fixation of certain joints e.g., fingers, elbows, knees, and hips in a flexed position contractures ; abnormally long, slender fingers and toes arachnodactyly ; permanently flexed fingers camptodactyly ; and/or abnormally shaped .CCA; Beals Syndrome; Beals-Hecht syndrome; Arthrogryposis, Distal, Type 9 Additional common symptoms include abnormally long, slender fingers and toes arachnodactyly , permanently flexed fingers camptodactyly , underdevelopment of certain muscles muscular hypoplasia , and front-to-back and side-to-side .
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