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Hepatomegalia
Hepatomegaly
Hepatomegaly NOS
Hepatomegaly and splenomegaly
Liver enlargement
Malformation of liver NOS
Polycoric hepatomegaly

Traduction de «Polycoric hepatomegaly » (Anglais → Néerlandais) :



A rare autosomal recessively inherited disorder of ketone body metabolism, characterized clinically by episodes of decompensation (often associated with gastroenteritis or fasting) that present with vomiting, lethargy, hepatomegaly, non ketotic hypog

deficiëntie van 3-hydroxy-3-methylglutaryl-co-enzym-A-synthase


A rare genetic gastroenterological disease characterized by the early onset of chronic diarrhea, vomiting, anorexia, lactic acidosis, renal insufficiency and hepatic involvement (mild elevation of liver enzymes, steatosis, hepatomegaly). Partial vill

syndroom van chronische diarree met villusatrofie


A rare genetic mitochondrial DNA depletion syndrome characterized by neonatal or early-infantile onset hepatopathy (manifesting with hepatomegaly, cholestasis, increased transaminases, coagulopathy, hypoalbuminemia, ascites, and/or liver failure), as

hepatocerebrorenale vorm van mitochondriaal DNA-depletiesyndroom


hepatomegaly | liver enlargement

hepatomegalie | leververgroting


hepatomegalia | hepatomegaly

hepatomegalia | hepatomegalie | leververgroting




Hepatomegaly and splenomegaly

hepatomegalie en splenomegalie


Accessory liver Alagille's syndrome Congenital:absence of liver | hepatomegaly | malformation of liver NOS

accessoire lever | congenitale | hepatomegalie | congenitale | misvorming van lever NNO | congenitale | ontbreken van lever | syndroom van Alagille




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'Polycoric hepatomegaly' ->

Date index: 2021-07-27
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