Acrocallosal syndrome

Acrocallosal syndrome
OMIM	200990
MeSH	D055673

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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.

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Template:Congenital malformations and deformations of nervous system