dyskeratosis

dyskeratosis
дискератоз

Англо-русский офтальмологический словарь. 2010.

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Смотреть что такое "dyskeratosis" в других словарях:

  • Dyskeratosis congenita — An inherited cause of bone marrow failure, dyskeratosis congenita is a syndrome characterized by abnormal excess skin pigmentation, abnormal or absent nails, and mucosal leukoplakia (white premalignant areas on the lips and conjunctiva of the… …   Medical dictionary

  • Dyskeratosis congenita — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 30105 ICD10 = ICD10|Q|82|8|q|80 ICD9 = ICD9|757.39 ICDO = OMIM = 305000 MedlinePlus = eMedicineSubj = derm eMedicineTopic = 111 MeshID = D019871Dyskeratosis congenita (DKC), also called… …   Wikipedia

  • Dyskeratosis bullosa hereditaria — Klassifikation nach ICD 10 Q82.8 Sonstige näher bezeichnete angeborene Fehlbildungen der Haut …   Deutsch Wikipedia

  • dyskeratosis — noun Incomplete or abnormal keratinization occurring prematurely within individual cells or groups of cells below the stratum granulosum …   Wiktionary

  • dyskeratosis — 1. Premature keratinization in individual epithelial cells that have not reached the keratinizing surface layer; dyskeratotic cells generally become rounded and they may break away from adjacent cells and fall off. 2. Epidermalization of the… …   Medical dictionary

  • dyskeratosis — dys·keratosis …   English syllables

  • dyskeratosis — …   Useful english dictionary

  • Dyskeratosis maligna — Morbus Bowen; Bowen Hautkrebs; Dermatosis praecancerosa Bowen (fachsprachlich); Bowen Karzinom; Erythroplasie de Queyrat (fachsprachlich) …   Universal-Lexikon

  • Dyskeratosis follicularis — Morbus Darier …   Universal-Lexikon

  • Syndrome, dyskeratosis congenita — An inherited cause of bone marrow failure, dyskeratosis congenita is a syndrome characterized by abnormal excess skin pigmentation, abnormal or absent nails, and mucosal leukoplakia (white premalignant areas on the lips and conjunctiva of the… …   Medical dictionary

  • hereditary benign intraepithelial dyskeratosis — an autosomal dominant disorder caused by mutation at 4q35, characterized by foamy gelatinous plaques on the conjunctiva and white thickenings resembling leukoplakia on the oral mucosa; photophobia is common in children, and blindness may occur.… …   Medical dictionary


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