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lüll Beals-Hecht syndrome Jones JL; Lane JE; Logan JJ; Vanegas MESouth Med J 2002[Jul]; 95 (7): 753-5Beals-Hecht syndrome, also known as congenital contractural arachnodactyly, is caused by a defect in fibrillin as in Marfan syndrome. This syndrome is characterized by a multitude of clinical findings including arachnodactyly, narrow body habitus, scoliosis, congenital contractures, and external ear deformities. Restrictive lung disease may be associated with the severe scoliosis and thoracic cage abnormalities in this syndrome. We describe a child with Beals-Hecht syndrome and review the literature.|Child[MESH]|Connective Tissue Diseases/*diagnosis/genetics[MESH]|Contracture/congenital/*diagnosis/genetics[MESH]|Ear, External/abnormalities[MESH]|Fibrillins[MESH]|Genes, Dominant[MESH]|Humans[MESH]|Lung Diseases/diagnosis/genetics[MESH]|Male[MESH]|Microfilament Proteins/deficiency[MESH]|Scoliosis/diagnosis/genetics[MESH]|Somatotypes[MESH]|Syndrome[MESH] |