Crigler
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Crigler–Najjar syndrome — Classification and external resources Bilirubin ICD 10 E80.5 … Wikipedia
Crigler-Najjar syndrome — Crigler Najjar syndrome. См. врожденная негемолитическая желтуха. (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.
Crigler-Najjar syndrome — DiseaseDisorder infobox Name = Crigler Najjar Syndrome ICD10 = ICD10|E|80|5|e|70 ICD9 = ICD9|277.4 ICDO = Caption = Bilirubin OMIM = 218800 OMIM mult = OMIM2|606785 MedlinePlus = 001127 eMedicineSubj = med eMedicineTopic = 476 DiseasesDB = 3176… … Wikipedia
Crigler-Najjar-Syndrom — Klassifikation nach ICD 10 E80.5 Crigler Najjar Syndrom … Deutsch Wikipedia
Crigler-Najjar Syndrom — Klassifikation nach ICD 10 E80.5 Crigler Najjar Syndrom … Deutsch Wikipedia
Crigler-Najjar syndrome — a genetic disease in which the liver enzyme glucuronyl transferase, responsible for dealing with bilirubin, is absent. Large amounts of bilirubin accumulate in the blood, and the child becomes progressively more jaundiced. The only treatment is a … Medical dictionary
Crigler-Najjar syndrome — a genetic disease in which the liver enzyme glucuronyl transferase, responsible for dealing with bilirubin, is absent. Large amounts of bilirubin accumulate in the blood, and the child becomes progressively more jaundiced. The only treatment is a … The new mediacal dictionary
Síndrome de Crigler-Najjar — Molécula de bilirrubina. Clasificación y recursos externos CIE 10 E80.5 … Wikipedia Español
Syndrôme de Crigler Najjar — Le syndrome de Criggler Najjar est une maladie génétique qui doit son nom aux deux médecins américains Criggler et Najjar qui le découvrirent dans les années 1950. C est une maladie rare qui sans traitement palliatif entraine rapidement la mort… … Wikipédia en Français
síndrome de CRIGLER-NAJJAR — Presencia de bilirrubina no conjugada en sangre de 20 a 45 mg/dl que aparece en el período neonatal y persiste toda la vida. Existen dos tipos: CN 1 y CN 2. Se trata de una enfermedad hereditaria producida por mutaciones en el gen UGT1 (que… … Diccionario médico
