Griscelli syndrome

Griscelli syndrome. Type two Griscelli syndrome is caused by the loss of Rab27. It has completely different symptoms from Choroideremia
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Choroideremia Research Foundation ...

Griscelli syndrome, also inherited in an autosomal recessive manner, was originally described as decreased cutaneous pigmentation with hypomelanosis and neurologic deficits, but its clinical presentation is quite variable.

Hematopoietic SCT in children with Griscelli syndrome: a single-center experience. Bone… more…
Primary Immune Deficiency Disease… ...

chronic infantile neurologic, cutaneous, and articular syndrome
chronic neurologic, cutaneous, and articular syndrome
CINCA
CINCA syndrome
infantile onset multisystem inflammatory disease
IOMID syndrome
Prieur-Griscelli syndrome ...

cold skin
Griscelli disease ... fever
Griscelli syndrome type II ... fever
Groin Hernia ... fever
Guanarito virus ... fever
Guillain-Barre Syndrome ... fever
Gynephobia ... trembling
Gynophobia ... trembling ...

See also: Dystrophy, Symptom, Deficiency, Rash, Ectodermal dysplasia