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Griscelli syndrome

MONDO:0018306

Griscelli syndrome (GS) is characterized by silvery gray sheen of the hair and hypopigmentation of the skin which can be associated to neurological impairment (type 1), immunodeficiency (type 2) or be isolated (type 3).

Also known as: ChC)diak-Higashi-like syndrome, Chédiak-Higashi-like syndrome, Ch��diak-Higashi-like syndrome, Griscelli-PruniC)ras syndrome, Griscelli-Pruniéras syndrome, Griscelli-Pruni��ras syndrome, partial albinism-immunodeficiency syndrome, Griscelli disease

33 clinical trials for this condition and its sub-types.

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Sub-types

Griscelli syndrome type 2 (1) Griscelli syndrome type 1 (0) Griscelli syndrome type 3 (0)

Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Skin disorder (123) Inborn errors of metabolism (42) Syndromic disease (24) Human disease (14) Skin pigmentation disorder (11) Hereditary skin disorder (5) Disease of genetic or genomic mechanism (2)
Trials to join now! 17 Not yet recruiting 4 Not yet finished but already full! 5 Completed 7
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