Other terms
Syndrome, Weill-Marchesani,Mesodermal Dysmorphodystrophy, Congenital,Congenital Mesodermal Dysmorphodystrophies,Congenital Mesodermal Dysmorphodystrophy,Dysmorphodystrophies, Congenital Mesodermal,Dysmorphodystrophy, Congenital Mesodermal,Mesodermal Dysmorphodystrophies, Congenital,Weill Marchesani Syndrome,Marchesani-Weill Syndrome,Marchesani Weill Syndrome,Marchesani-Weill Syndromes,Syndrome, Marchesani-Weill,Syndromes, Marchesani-Weill,Spherophakia Brachymorphia Syndrome,Brachymorphia Syndrome, Spherophakia,Spherophakia Brachymorphia Syndromes,Syndrome, Spherophakia Brachymorphia,Syndromes, Spherophakia Brachymorphia,Weill-Marchesani Syndrome, Autosomal Dominant,Weill Marchesani Syndrome, Autosomal Dominant,Weill-Marchesani Syndrome, Autosomal Recessive,Weill Marchesani Syndrome, Autosomal Recessive
Description
Weill-Marchesani Syndrome: Rare congenital disorder of connective tissue characterized by brachydactyly, joint stiffness, childhood onset of ocular abnormalities (e.g., microspherophakia, ECTOPIA LENTIS; GLAUCOMA), and proportionate short stature. Cardiovascular anomalies are occasionally seen.
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