Intrahepatisk galdesten hos en patient med alkaptonuri

Charlotte Bülow; Jacob Rosenberg

Intrahepatisk galdesten hos en patient med alkaptonuri

2 Citationer (Scopus)

Abstract

Alkaptonuria is a rare inherited disease with enzyme deficiency in the protein metabolism. The patients accumulate homogentisic acid which leads to symptoms from various body tissues. We describe a patient with recurrent intrahepatic gallstones probably due to such accumulation, and the successful treatment with removal of the stones and a low-protein diet.
Udgivelsesdato: 2009-Jun

Bidragets oversatte titel	Intrahepatic gallstones in patient with alkaptonuria
Originalsprog	Dansk
Tidsskrift	Ugeskrift for læger
Vol/bind	171
Udgave nummer	26
Sider (fra-til)	2198-9
Antal sider	2
ISSN	0041-5782
Status	Udgivet - 2009

Citationsformater

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title = "Intrahepatisk galdesten hos en patient med alkaptonuri",

abstract = "Alkaptonuria is a rare inherited disease with enzyme deficiency in the protein metabolism. The patients accumulate homogentisic acid which leads to symptoms from various body tissues. We describe a patient with recurrent intrahepatic gallstones probably due to such accumulation, and the successful treatment with removal of the stones and a low-protein diet. Udgivelsesdato: 2009-Jun",

author = "Charlotte B{\"u}low and Jacob Rosenberg",

note = "Keywords: Alkaptonuria; Bile Ducts, Intrahepatic; Diet, Protein-Restricted; Female; Gallstones; Humans; Middle Aged; Recurrence",

year = "2009",

language = "Dansk",

volume = "171",

pages = "2198--9",

journal = "Ugeskrift for Laeger",

issn = "0041-5782",

publisher = "Almindelige Danske Laegeforening",

number = "26",

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TY - JOUR

T1 - Intrahepatisk galdesten hos en patient med alkaptonuri

AU - Bülow, Charlotte

AU - Rosenberg, Jacob

N1 - Keywords: Alkaptonuria; Bile Ducts, Intrahepatic; Diet, Protein-Restricted; Female; Gallstones; Humans; Middle Aged; Recurrence

PY - 2009

Y1 - 2009

N2 - Alkaptonuria is a rare inherited disease with enzyme deficiency in the protein metabolism. The patients accumulate homogentisic acid which leads to symptoms from various body tissues. We describe a patient with recurrent intrahepatic gallstones probably due to such accumulation, and the successful treatment with removal of the stones and a low-protein diet. Udgivelsesdato: 2009-Jun

AB - Alkaptonuria is a rare inherited disease with enzyme deficiency in the protein metabolism. The patients accumulate homogentisic acid which leads to symptoms from various body tissues. We describe a patient with recurrent intrahepatic gallstones probably due to such accumulation, and the successful treatment with removal of the stones and a low-protein diet. Udgivelsesdato: 2009-Jun

M3 - Tidsskriftartikel

C2 - 19671401

SN - 0041-5782

VL - 171

SP - 2198

EP - 2199

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

IS - 26

ER -