|Classification and external resources|
Elejalde syndrome (also known as "Griscelli syndrome type 1") is a rare autosomal recessive syndrome consisting of moderate pigment dilution, profound primary neurologic defects, no immune defects, and hair with metallic silvery sheen.:866
It is associated with MYO5A.
- James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
See also: cytoskeletal proteins
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