MeSH 搜索器

Chediak-Higashi Syndrome

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.
推出的年份: 1971
副标题
树号: C11.270.040.772, C15.378.553.774.257, C16.320.798.375, C20.673.774.257, C20.673.795.375
MeSH 单一 ID: D002609
进入的组:
  • Chediak Higashi Syndrome
  • Oculocutaneous Albinism with Leukocyte Defect
  • Chediak-Steinbrinck-Higashi Syndrome
  • Chediak Steinbrinck Higashi Syndrome
  • Chediak-Steinbrinck-Higashi Syndromes
早前的内容:
  • Immunologic Deficiency Syndromes (1968-1970)
  • Leukocytes (1966-1970)

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