Structured Summary
Abstract
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.
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Synonyms
5 entry terms
- Chediak-Steinbrinck-Higashi Syndrome
- Oculocutaneous Albinism with Leukocyte Defect
- Chediak Higashi Syndrome
- Chediak Steinbrinck Higashi Syndrome
- Chediak-Steinbrinck-Higashi Syndromes
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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History Note
71
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Previous Indexing
- Immunologic Deficiency Syndromes (1968-1970)
- Leukocytes (1966-1970)
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NLM Classification
QW 740
AMA Style
References
- National Library of Medicine. Chediak-Higashi Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D002609. http://id.nlm.nih.gov/mesh/2026/D002609
- Chediak-Higashi Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Ch%C3%A9diak%E2%80%93Higashi_syndrome
- Chediak-Higashi Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q934034