It is possible that the main title of the record Beals Syndrome is not the name you expected. Please inspect the words noting to find the alternating name(s) and problem neighborhood(s) covered by this record.
- arachnodactyly, contractural Beals type
- Beals-Hecht syndrome
- contractural arachnodactyly, hereditary
Beals syndrome is an incredibly rare congenital disease defined by the permanent fixation of certain joints (e.g., fingers, elbow joints, knees, and hips) in a flexed position (contractures); unusually long, slender fingers as well as toes (arachnodactyly); completely flexed fingers (camptodactyly); and/or uncommonly shaped ears resulting in a “messed up” look. Furthermore, impacted people could show front-to-back and side-to-side curvature of the spinal column (kyphoscoliosis); feet that are abnormally placed (talipes equinovarus or clubfoot); external displacement of the fingers (ulnar deviation of the fingers); an unusually brief neck; and/or. Seldom, impacted people could have a small deformity of the shutoff on the left side of the heart (mitral shutoff prolapse). Beals disorder is inherited as an autosomal leading attribute.