Acrocallosal syndrome

Acrocallosal syndrome
OMIM	200990
MeSH	D055673

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Acrocallosal syndrome (also known as ACLS) is a rare autosomal recessive syndrome characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental retardation, and other symptoms. The syndrome was first described by Albert Schinzel in 1979.

External links

• Template:RareDiseases

Template:Congenital malformations and deformations of nervous system