chediak higashi syndrome
1Chédiak–Higashi syndrome — Classification and external resources ICD 10 E70.3 (E70.340 ILDS) ICD 9 288.2 …
2Chediak-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.) …
3Chediak-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… …
4Chédiak-Higashi syndrome — ▪ pathology 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… …
5Chediak-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… …
6Chediak-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… …
7chediak-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 …
8Chediak-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… …
9Syndrome de Chediak-Higashi — Autre nom Référence MIM …
10Syndrome de chediak higashi — Autre nom Référence MIM …
