Basel-Vanagaite-Smirin-Yosef syndrome

Orpha code: 464738OMIM code: 616449

Definicja

A rare, genetic intellectual disability syndrome characterized by severe global developmental delay with intellectual disability, microcephaly, growth retardation, ocular defects such as congenital cataract, and nevus flammeus simplex on the forehead. Cardiac, urogenital, and skeletal abnormalities, as well as seizures are present in most patients. Dysmorphic craniofacial features include sparse hair, downslanting palpebral fissures, hypertelorism, broad and overhanging nasal tip and short philtrum, among others.

Disease data
Klasyfikacja

Malformation syndrome

Kod ORPHA
464738
Kod OMIM
616449
Kod ICD10
-
Kod ICD11
-

No additional description.

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