Chédiak-Higashi syndrome

Chédiak-Higashi syndrome

      a rare inherited childhood disease characterized by the inability of white blood cells called phagocytes to destroy invading microorganisms.

      Persons with Chédiak-Higashi syndrome experience persistent or recurrent infections. Other symptoms associated with the disease include enlargement of the liver and spleen, partial albinism, and depressed activity of other cells, called natural killer cells, that are involved in defending the body against infection.

      The inability of phagocytes to kill infectious microorganisms is caused by a defect in a gene that controls the formation of vesicles inside phagocytic cells. Normally phagocytes eliminate microorganisms through a process called phagocytosis, a type of cellular “eating,” in which the phagocyte engulfs and digests a microbe by means of chemicals contained in its vesicles. In individuals with Chédiak-Higashi syndrome, the phagocytes have large, abnormally formed vesicles that make the cells more rigid, less mobile, and unable to destroy microorganisms.

      Chédiak-Higashi syndrome is inherited in an autosomal recessive manner (meaning that a child must inherit a copy of the gene responsible for the disease from both parents). Only 200 total cases of the disease have been reported in humans. Persons with this disorder are usually recognized early in life, and few survive to adulthood. Treatments for the disease include long-term antibiotic therapy, bone marrow transplants, and white blood cell or whole blood transfusions. A similar disorder has been observed in mice, Hereford cattle, killer whales, blue smoke Persian cats, and mink.

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Universalium. 2010.

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Look at other dictionaries:

  • Chédiak–Higashi syndrome — Classification and external resources ICD 10 E70.3 (E70.340 ILDS) ICD 9 288.2 …   Wikipedia

  • Chediak-Higashi syndrome — Chediak Higashi syndrome. См. синдром Чедиак Хигаши. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) …   Молекулярная биология и генетика. Толковый словарь.

  • Chediak-Higashi syndrome — Infobox Disease Name = Chédiak Higashi syndrome Caption = DiseasesDB = 2351 ICD10 = ICD10|E|70|3|e|70 (E70.340 ILDS) ICD9 = ICD9|288.2 ICDO = OMIM = 214500 MedlinePlus = eMedicineSubj = derm eMedicineTopic = 704 MeshID = D002609 Chédiak Higashi… …   Wikipedia

  • Chediak-Higashi syndrome — Che·diak Hi·ga·shi syndrome shād .yäk hē .gäsh ē n a genetic disorder inherited as an autosomal recessive and characterized by partial albinism, abnormal granules in the white blood cells, and marked susceptibility to bacterial infections… …   Medical dictionary

  • Chediak-Higashi syndrome — a rare fatal hereditary disease in children, inherited as an autosomal recessive condition, causing enlargement of the liver and spleen, albinism, and abnormalities of the eye. The cause is unknown but thought to be due to a disorder of… …   The new mediacal dictionary

  • chediak-higashi syndrome — shād¦yäkhē¦gäshē noun Usage: usually capitalized C&H Etymology: after Moises Chediak fl1952 French physician and Ototaka Higashi fl1954 Jap. physician : a genetic disorder inherited as an autosomal recessive and characterized by partial albinism …   Useful english dictionary

  • Chediak-Higashi syndrome — Autosomal recessive disorder characterized by the presence of giant lysosomal vesicles in phagocytes and in consequence poor bactericidal function. Some perturbation of microtubule dynamics seems to be involved. Reported from humans, albino… …   Dictionary of molecular biology

  • Syndrome de Chediak-Higashi — Autre nom Référence MIM …   Wikipédia en Français

  • Syndrome de chediak higashi — Autre nom Référence MIM …   Wikipédia en Français

  • Syndrome de Chediak Higashi — Référence MIM 214500 Transmission Récessive Chromosome 1q42.1 q42.2 Gène LYST Nombre d allèles pathologiques …   Wikipédia en Français

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