ectodermal dysplasia

ectodermal dysplasia
Медицина: врождённая эктодермальная дисплазия, эктодермальная дисплазия, врождённый эктодермальный дефект (врожденное недоразвитие эпидермиса и придатков кожи, отсутствие или гипоплазия волос, дистрофия ногтей, аплазия и дистрофия зубов, вазомоторные рефлексы понижены)

Универсальный англо-русский словарь. . 2011.

Смотреть что такое "ectodermal dysplasia" в других словарях:

  • Ectodermal dysplasia — Classification and external resources ICD 10 Q82.4 ICD 9 757.31 …   Wikipedia

  • Ectodermal dysplasia — A genetic disorder in which there is abnormal development of the skin and associated structures (the hair, nails, teeth, and sweat glands). The most dangerous problem occurs in cases with decreased sweating due to absence of the sweat glands.… …   Medical dictionary

  • Ectrodactyly-ectodermal dysplasia-cleft syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 34402 ICD10 = ICD9 = ICDO = OMIM = 129900 OMIM mult = OMIM2|604292 | MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Ectrodactyly ectodermal dysplasia cleft syndrome, or EEC, is a… …   Wikipedia

  • Hypohidrotic ectodermal dysplasia — Classification and external resources ICD 10 Q82.4 ICD 9 757.31 …   Wikipedia

  • Clouston's hidrotic ectodermal dysplasia — Classification and external resources OMIM 129500 Clouston s hidrotic ectodermal dysplasia (also known as Alopecia congenita with keratosis palmoplantaris, Clouston syndrome, [1] …   Wikipedia

  • anhidrotic ectodermal dysplasia — a genetically heterogeneous disorder characterized by ectodermal dysplasia associated with aplasia or hypoplasia of the sweat glands, hypothermia, alopecia, missing or conical teeth, and typical facies (frontal bossing, midfacial hypoplasia,… …   Medical dictionary

  • hypohidrotic ectodermal dysplasia — anhidrotic ectodermal d …   Medical dictionary

  • autoimmune polyendocrinopathy-candidiasis–ectodermal dysplasia — (APECED) polyendocrine autoimmune syndrome, type I …   Medical dictionary

  • hidrotic ectodermal dysplasia — an autosomal dominant disorder caused by mutations in the GJB6 gene (locus: 13q12), which encodes connexin 30. It is characterized by hypotrichosis; dystrophic, hypoplastic, or absent nails; hyperpigmentation of the skin over joints;… …   Medical dictionary

  • Dysplasia — Abnormal in form. From the Greek dys (bad, disordered, abnormal) and plassein (to form). For example, retinal dysplasia is abnormal formation of the retina during embryonic development. * * * Abnormal tissue development. SEE ALSO: heteroplasia.… …   Medical dictionary

  • Oculodentodigital dysplasia — Classification and external resources OMIM 164200 DiseasesDB 32980 Oculodentodigital syndrome (ODD syndrome) is an extremely rare genetic conditio …   Wikipedia


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