Alström
Carl-Henry, Swedish geneticist, *1907. See A. syndrome.

Medical dictionary. 2011.

Look at other dictionaries:

  • Alström-Syndrom — Klassifikation nach ICD 10 Q87.8 Sonstige näher bezeichnete angeborene Fehlbildungssyndrome, anderenorts nicht klassifiziert Alström Syndrom …   Deutsch Wikipedia

  • Alstrom syndrome — Infobox Disease Name = Alstrom syndrome Caption = DiseasesDB = 465 ICD10 = ICD9 = ICDO = OMIM = 203800 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Alström syndrome is a rare genetic disorder. It is among the rarest genetic disorders… …   Wikipedia

  • Alstrom syndrome — A progressive genetic disorder characterized by obesity, deafness, and visual problems in childhood and diabetes with insulin resistance (type 2 diabetes) and kidney failure in adulthood. Individuals with Alström syndrome have been identified in… …   Medical dictionary

  • Alström`s warbler — Alstriomo raštuotoji pečialinda statusas T sritis zoologija | vardynas atitikmenys: lot. Seicercus soror angl. Alström s warbler vok. Thailaubsänger, m pranc. pouillot soeur, m ryšiai: platesnis terminas – raštuotosios pečialindos …   Paukščių pavadinimų žodynas

  • Alstrom, Bo — (1937 ) (Sweden)    History painter based in Sigtuna, Sweden. Studied at Uppsala University.    Reproductions: Goan; 1969; oil on canvas; Philips, 1979: fig. 46 [B] …   Dictionary of erotic artists: painters, sculptors, printmakers, graphic designers and illustrators

  • Syndrome d'Alstrom — Syndrome d Alström Syndrome d Alström Autre nom {{{Autre nom}}} Référence MIM 2 …   Wikipédia en Français

  • Síndrome de Alström — Imagen transaxial del torax a nivel del corazón, ilustrando la típica capa de tejido adiposo subcutáneo y epicárdico (en blanco) en un paciente con este síndrome …   Wikipedia Español

  • Carl-Henry Alström — (1907 1993) was a Swedish psychiatrist who described a syndrome now named for him, Alström syndrome, an hereditary disorder that characteristically includes obesity in childhood, nerve deafness and retinal degeneration (due to atypical retinitis… …   Wikipedia

  • Syndrome d'Alström — Référence MIM 203800 Transmission Récessive Chromosome 2 p13 Gène ALMS1 Empreinte parentale Non …   Wikipédia en Français

  • síndrome de ALSTRÖM-HALLGREN — un síndrome parecido al de Laurence Moon Biedl Bardet que se manifiesta por obesidad en la infancia, sordera nerviosa y degeneración de la retina ( retinitis pigmentosa atípica). La ceguera ocurre usualmente a los 7 años. La condición va… …   Diccionario médico

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