Muscular Dystrophy, Congenital, Davignon-Chauveau Type, is also known as congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome. An important gene associated with Muscular Dystrophy, Congenital, Davignon-Chauveau Type is TRIP4 (Thyroid Hormone Receptor Interactor 4). Affiliated tissues include skin and skeletal muscle, and related phenotypes are emg: myopathic abnormalities and respiratory insufficiency due to muscle weakness