Intrahepatisk galdesten hos en patient med alkaptonuri

Charlotte Bülow; Jacob Rosenberg

Intrahepatisk galdesten hos en patient med alkaptonuri

Translated title of the contribution: Intrahepatic gallstones in patient with alkaptonuria

2 Citations (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

Translated title of the contribution	Intrahepatic gallstones in patient with alkaptonuria
Original language	Danish
Journal	Ugeskrift for læger
Volume	171
Issue number	26
Pages (from-to)	2198-9
Number of pages	2
ISSN	0041-5782
Publication status	Published - 2009

Cite this

@article{8af31d80829911df928f000ea68e967b,

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",

}

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 -