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Acrocallosal syndrome

Introduction

Overview

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.[1] The syndrome was first described by Albert Schinzel in 1979.[2]

References

References

External links


Template:Congenital malformations and deformations of nervous system

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