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Chediak-Higashi Syndrome

More information in Books or onNLM PubMed
Definition: A form of phagocyte bactericidal dysfunction characterized by unusual oculocutaneous albinism, high incidence of lymphoreticular neoplasms, and recurrent pyogenic infections. In many cell types, abnormal lysosomes are present leading to defective pigment distribution and abnormal neutrophil functions. The disease is transmitted by autosomal recessive inheritance and a similar disorder occurs in the beige mouse, the Aleutian mink, and albino Hereford cattle.  "a form of phagocyte bactericidal dysfunct"   
See Also Aleutian Mink Disease
Other names Syndrome, Chediak-Higashi; Chediak Higashi Syndrome
 
SubstanceCAS Registry & nameCategoriesSource
Neutropenia and hyperlymphocytosis with large granular lymphocytes  0   *Chediak-Higashi Syndrome.
NBEA protein, human  0   *Carrier Proteins *Nerve Tissue Proteins Chediak-Higashi Syndrome Membrane Proteins.
Nbea protein, mouse  0   *Carrier Proteins *Nerve Tissue Proteins Chediak-Higashi Syndrome Membrane Proteins. Mamm Genome 1999 Oct;10(10):1030-1

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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