Transient carnitine transport defect with cholestatic jaundice: report of one case in a premature baby
Carnitine (β-hydroxy-γ-trimethylaminobutyric acid) is involved in the transport of long-chain fatty acids into the mitochondrial matrix and the removal of potentially toxic acylcarnitine esters. Transient carnitine transport defect is a rare condition in newborns reported in 1/90,000 live births. In...
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Published in | Clinical and experimental pediatrics Vol. 55; no. 2; pp. 58 - 62 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
Clinical and Experimental Pediatics / Korean Pediatric Society
01.02.2012
The Korean Pediatric Society Korean Pediatric Society 대한소아청소년과학회 |
Subjects | |
Online Access | Get full text |
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Summary: | Carnitine (β-hydroxy-γ-trimethylaminobutyric acid) is involved in the transport of long-chain fatty acids into the mitochondrial matrix and the removal of potentially toxic acylcarnitine esters. Transient carnitine transport defect is a rare condition in newborns reported in 1/90,000 live births. In this paper, we describe a case of transient carnitine transport defect found in a premature baby who had prolonged cholestatic jaundice and poor weight gain, and who responded dramatically to oral carnitine supplementation. |
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Bibliography: | G704-000560.2012.55.2.002 |
ISSN: | 1738-1061 2092-7258 2713-4148 |
DOI: | 10.3345/kjp.2012.55.2.58 |