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
相关论文
共 50 条
  • [31] Maternal metabolic defects detected through expanded newborn screening in Catalonia
    Pajares, S.
    Lopez, R. M.
    Argudo, A.
    De Aledo-Castillo, J. M. Gonzalez
    Marin, J. L.
    Garcia, J.
    Flores, E.
    Martinez, C.
    Arranz, J. A.
    Artuch, R.
    Ormazabal, A.
    Del Toro, M.
    Garcia-Cazorla, A.
    Meavilla, S.
    Fernandez-Bordon, R. M.
    Ribes, A.
    [J]. CLINICA CHIMICA ACTA, 2019, 493 : S602 - S603
  • [32] Expanded Newborn Screening for Detection of Vitamin B12 Deficiency
    Sarafoglou, Kyriakie
    Rodgers, John
    Hietala, Amy
    Matern, Dietrich
    Bentler, Kristi
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2011, 305 (12): : 1198 - 1200
  • [33] Neonatal vitamin B12 deficiency secondary to maternal subclinical pernicious anemia:: Identification by expanded newborn screening
    Marble, Michael
    Copeland, Sara
    Khanpar, Nashat
    Rosenblatt, David S.
    [J]. JOURNAL OF PEDIATRICS, 2008, 152 (05): : 731 - 733
  • [34] Carnitine-Palmitoyltransferase 2 Deficiency: Novel Mutations and Relevance of Newborn Screening
    Illsinger, Sabine
    Luecke, Thomas
    Peter, Michael
    Ruiter, Jos P. N.
    Wanders, Ronald J. A.
    Deschaner, Marcus
    Handig, Ingrid
    Wuyts, Wim
    Das, Anibh M.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (22) : 2925 - 2928
  • [35] Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death
    Najim Lahrouchi
    Elisabeth M Lodder
    Maria Mansouri
    Rafik Tadros
    Layla Zniber
    Najlae Adadi
    Sally-Ann B Clur
    Karin Y van Spaendonck-Zwarts
    Alex V Postma
    Abdelaziz Sefiani
    Ilham Ratbi
    Connie R Bezzina
    [J]. European Journal of Human Genetics, 2017, 25 : 783 - 787
  • [36] A qualitative study on the perspectives of mothers who had been diagnosed with primary carnitine deficiency through newborn screening of their child
    Lieke M. van den Heuvel
    Adriana Kater-Kuipers
    Tessa van Dijk
    Loek L. Crefcoeur
    Gepke Visser
    Mirjam Langeveld
    Lidewij Henneman
    [J]. Orphanet Journal of Rare Diseases, 18
  • [37] Newborn Screening and Genetic Analysis Identify Six Novel Genetic Variants for Primary Carnitine Deficiency in Ningbo Area, China
    Yang, Xiangchun
    Li, Qiong
    Wang, Fei
    Yan, Lulu
    Zhuang, Danyan
    Qiu, Haiyan
    Li, Haibo
    Chen, Liang
    [J]. FRONTIERS IN GENETICS, 2021, 12
  • [38] Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening (vol 16, 503, 2021)
    Lin, Yiming
    Lin, Bangbang
    Chen, Yanru
    Zheng, Zhenzhu
    Fu, Qingliu
    Lin, Weihua
    Zhang, Weifeng
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2022, 17 (01)
  • [39] A qualitative study on the perspectives of mothers who had been diagnosed with primary carnitine deficiency through newborn screening of their child
    van den Heuvel, Lieke M. M.
    Kater-Kuipers, Adriana
    van Dijk, Tessa
    Crefcoeur, Loek L. L.
    Visser, Gepke
    Langeveld, Mirjam
    Henneman, Lidewij
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2023, 18 (01)
  • [40] PRIMARY CARNITINE DEFICIENCY
    SCHOLTE, HR
    PEREIRA, RR
    DEJONGE, PC
    LUYTHOUWEN, IEM
    VERDUIN, MHM
    ROSS, JD
    [J]. JOURNAL OF CLINICAL CHEMISTRY AND CLINICAL BIOCHEMISTRY, 1990, 28 (05): : 351 - 357