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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...
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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...
- blue rats, mice, minks, foxes, and the only
known captive white orca.
Griscelli syndrome (also
known as "Chédiak–Higashi like syndrome") Rapini, Ronald...
- 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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melanosome trafficking. It is ****ociated with MYO5A.[citation needed]
Griscelli syndrome James, William; Berger, Timothy; Elston, Dirk (2005). Andrews'...
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children and adolescents. It was
created in 1989 by
professor Claude Griscelli and
backed by the
Fondation des Hôpitaux. One of the foundation's main...
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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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Griscelli syndrome type 3 is a
disorder of
melanosome transport presenting initially with hypopigmentation.: 866
Griscelli syndrome James, William; Berger...
