Basel-Vanagaite-Smirin-Yosef syndrome

Orpha code: 464738OMIM code: 616449

Definition

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
Classification

Malformation syndrome

ORPHA code
464738
OMIM code
616449
ICD10 code
-
ICD11 code
-

No additional description.

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