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Metaboliske levertilstande

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Overvej altid ved kronisk leversygdom /<br />

leversymptomer! – essentielt for behandlingen<br />

Hereditære<br />

Porfyrinstofskiftet<br />

• Porfyria cutanea tarda<br />

• Erytropoietisk protoporfyri<br />

Sukkerstofskiftet<br />

• Glycogen storage-sygdomme (Type 0-<br />

XI)<br />

• Galaktosæmi<br />

Glykoproteiner og glykolipider<br />

• Mucopolysakkaridose (Type I-VII)<br />

• Mucolipidose (Type I-IV)<br />

ER storage disease<br />

• α 1<br />

-antitrypsinmangel<br />

• α 1<br />

-antichymotrypsinmangel<br />

• Hypofibrinogenæmi<br />

Aminosyrestofskiftet<br />

• Tyrosinæmi<br />

Lipoproteiner og lipidstofskiftet<br />

• Abetalipoproteinæmi<br />

• Familiær hypobetalipoproteinæmi<br />

• Familiær hyperkolesterolæmi<br />

• Kolesterolester storage disease<br />

• Fabry, Farber, Gaucher, Niemann-Pick<br />

Peroxisomale sygdomme<br />

• Zellweger, Refsum<br />

Mitochondriesygdomme<br />

• Pearson, Navajo neurohepatopati<br />

Kobberstofskiftet<br />

• Wilson<br />

Jernstofskiftet<br />

• Hæmokromatose (Type 1-4), neonatal<br />

HK<br />

Bilirubinstofskiftet<br />

• Benign recurrent intrahepatisk<br />

cholestase (BRIC), progressiv familiær<br />

intrahepatisk cholestase (PFIC)<br />

• Crigler-Najjar, Gilbert, Dubin-Johnson<br />

Andre<br />

• Cystisk fibrose, albinisme<br />

Erhvervede<br />

Adipositas<br />

Diabetes mellitus<br />

Metabolisk syndrom

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