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van den Ende-Gupta syndrome

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Van den Ende-Gupta syndrome is a very rare syndrome characterized by blepharophimosis, arachnodactyly, joint contractures, and characteristic dysmorphic features.
Uniprot Description A syndrome characterized by craniofacial and skeletal abnormalities that include blepharophimosis, a flat and wide nasal bridge, narrow and beaked nose, hypoplastic maxilla with or without cleft palate and everted lower lip, prominent ears, down-slanting eyes, arachnodactyly, and camptodactyly. Patients present congenital joint contractures that improve without intervention, and normal growth and development. Intelligence is normal. Rarely, enlarged cerebella can be present. Some patients experience respiratory problems due to laryngeal abnormalities.
Mondo Term and Equivalent IDs
MONDO:0010959:  van den Ende-Gupta syndrome
DOID:0111699: 
GARD:0003382: 
MESH:C535909: 
Orphanet:2460: 
SCTID:719845008: 
UMLS:C1833136: