Expanded newborn screening identifies maternal primary carnitine deficiency

被引:77
|
作者
Schimmenti, Lisa A.
Crombez, Eric A.
Schwahn, Bernd C.
Heese, Bryce A.
Wood, Timothy C.
Schroer, Richard J.
Bentler, Kristi
Cederbaum, Stephen
Sarafoglou, Kiki
McCann, Mark
Rinaldo, Piero
Matern, Dietrich
di San Filippo, Cristina Amat
Pasquali, Marzia
Berry, Susan A. [1 ]
Longo, Nicola
机构
[1] Univ Minnesota, Dept Pediat, Div Genet & Metab, Inst Human Genet, Minneapolis, MN 55455 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Genet & Metab, Los Angeles, CA 90095 USA
[3] Univ Dusseldorf, Childrens Hosp, Dept Gen Pediat, D-40225 Dusseldorf, Germany
[4] Mayo Clin & Mayo Fdn, Coll Med, Dept Lab Med & Pathol, Div Lab Genet, Rochester, MN 55905 USA
[5] Greenwood Genet Ctr, Greenwood, SC 29646 USA
[6] Minnesota Dept Hlth, Minneapolis, MN USA
[7] Univ Utah, Dept Pediat, Salt Lake City, UT USA
[8] Univ Utah, Dept Pathol, Salt Lake City, UT USA
[9] Univ Utah, ARUP Labs, Salt Lake City, UT USA
关键词
carnitine deficiency; newborn screening; sudden death; maternal disease; carnitine transport; OCTN2;
D O I
10.1016/j.ymgme.2006.10.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Primary carnitine deficiency impairs fatty acid oxidation and can result in hypoglycemia, hepatic encephalopathy, cardiomyopathy and sudden death. We diagnosed primary carnitine deficiency in six unrelated women whose unaffected infants were identified with low free carnitine levels (C0) by newborn screening using tandem mass spectrometry. Given the lifetime risk of morbidity or sudden death, identification of adult patients with primary carnitine deficiency is an added benefit of expanded newborn screening programs. (c) 2007 Published by Elsevier Inc.
引用
收藏
页码:441 / 445
页数:5
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