-
Griscelli syndrome is a rare
autosomal recessive disorder characterized by
albinism (hypopigmentation) with immunodeficiency, that
usually causes death...
- cell activity.[citation needed] A
major differential diagnosis of HLH is
Griscelli syndrome (type 2). This is a rare
autosomal recessive disorder characterized...
- blue rats, mice, minks, foxes, and the only
known captive white orca.
Griscelli syndrome (also
known as "Chédiak–Higashi like syndrome") Rapini, Ronald...
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disorders that
affect melanin production,
causing pale skin, hair, and eyes.
Griscelli syndrome: A rare
genetic condition characterized by
pigmentary dilution...
- Hermansky–Pudlak
syndrome Chédiak–Higashi
syndrome Griscelli syndrome Elejalde syndrome Griscelli syndrome type 2
Griscelli syndrome type 3
Other Cross syndrome ABCD...
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Griscelli syndrome type 2 (also
known as "partial
albinism with immunodeficiency") is a rare
autosomal recessive syndrome characterized by
variable cutenous...
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melanosome trafficking. It is ****ociated with MYO5A.[citation needed]
Griscelli syndrome James, William; Berger, Timothy; Elston, Dirk (2005). Andrews'...
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cephalopolysyndactyly syndrome Grinspan's
syndrome Griscelli syndrome type 2
Griscelli syndrome type 3
Griscelli syndrome Grisel's
syndrome Growing teratoma...
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Elejalde syndrome (
Griscelli syndrome type 1)
Eruptive hypomelanosis Familial progressive hyperpigmentation Galli–Galli
disease Griscelli syndrome type 2...
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treated with the drug anakinra. This
syndrome is also
known as the Prieur–
Griscelli syndrome as it was
first described by
these authors in 1981. The age of...
