Energy utilization issues in multiple acyl-CoA dehydrogenase deficiency type II (severe neonatal onset)

被引：0
|
作者：
Bannister, E. N. [1 ]
Arduini, K. J. [1 ]
机构：
[1] Ann & Robert H Lurie Childrens Hosp, Div Genet, Chicago, IL USA
来源：
MOLECULAR GENETICS AND METABOLISM | 2024年 / 141卷
关键词：
D O I：
10.1016/j.ymgme.2024.108407
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P.41
引用
收藏
页码：29 / 30
页数：2
相关论文
共 50 条
  • [41] Neonatal Ventricular Tachyarrhythmias in Medium Chain Acyl-CoA Dehydrogenase Deficiency
    Yusuf, Kamran
    Jirapradittha, Junya
    Amin, Harish J.
    Yu, Weiming
    Hasan, Shabih U.
    NEONATOLOGY, 2010, 98 (03) : 260 - 264
  • [42] Beneficial Effect of N-Carbamylglutamate in a Neonatal Form of Multiple Acyl-CoA Dehydrogenase Deficiency
    Stanescu, Sinziana
    Belanger-Quintana, Amaya
    Alcalde Martin, Carlos
    Perez-Cerda Silvestre, Celia
    Merinero Cortes, Begona
    Gonzalez Perez, Belen
    Fernandez Garcia-Abril, Carmen
    Arrieta Blanco, Francisco
    Palacios Valverde, Esperanza
    Martinez-Pardo Casanova, Mercedes
    CASE REPORTS IN PEDIATRICS, 2020, 2020
  • [43] LATE-ONSET MULTIPLE ACYL-COA DEHYDROGENASE-DEFICIENCY PRESENTING LIKE POLYMYOSITIS
    SANTOS, C
    CALDWELL, DS
    SANDERS, DB
    ANNALS OF NEUROLOGY, 1991, 30 (02) : 275 - 275
  • [44] Late-onset multiple acyl-CoA dehydrogenase deficiency with cardiac syncope: A case report
    Xue-Qi Pan
    Xue-Li Chang
    Wei Zhang
    Hua-Xing Meng
    Jing Zhang
    Jia-Ying Shi
    Jun-Hong Guo
    World Journal of Clinical Cases, 2020, (05) : 995 - 1001
  • [45] Late-onset multiple acyl-CoA dehydrogenase deficiency with cardiac syncope: A case report
    Pan, Xue-Qi
    Chang, Xue-Li
    Zhang, Wei
    Meng, Hua-Xing
    Zhang, Jing
    Shi, Jia-Ying
    Guo, Jun-Hong
    WORLD JOURNAL OF CLINICAL CASES, 2020, 8 (05) : 995 - 1001
  • [46] HEPATIC ACYL-COA PROFILES IN RIBOFLAVIN DEPRIVATION-INDUCED MULTIPLE ACYL-COA DEHYDROGENASE-DEFICIENCY
    STANLEY, CA
    CORKEY, BE
    BOOZ, G
    HALE, DE
    GLENNON, MC
    BERRY, GT
    PEDIATRIC RESEARCH, 1987, 21 (04) : A348 - A348
  • [47] GLUTARIC ACIDEMIA TYPE-II (MULTIPLE ACYL-COA DEHYDROGENATION DEFICIENCY)
    GOODMAN, SI
    FRERMAN, FE
    JOURNAL OF INHERITED METABOLIC DISEASE, 1984, 7 : 33 - 37
  • [48] A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report
    Loredana De Pasquale
    Petronilla Meo
    Francesco Fulia
    Antonio Anania
    Valerio Meli
    Antonina Mondello
    Maria Tindara Raimondo
    Viviana Tulino
    Maria Sole Coletta
    Caterina Cacace
    Italian Journal of Pediatrics, 48
  • [49] A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report
    De Pasquale, Loredana
    Meo, Petronilla
    Fulia, Francesco
    Anania, Antonio
    Meli, Valerio
    Mondello, Antonina
    Raimondo, Maria Tindara
    Tulino, Viviana
    Coletta, Maria Sole
    Cacace, Caterina
    ITALIAN JOURNAL OF PEDIATRICS, 2022, 48 (01)
  • [50] Short-chain acyl-CoA dehydrogenase deficiency associated with early onset severe axonal neuropathy
    Kurian, MA
    Hartley, L
    Zolkipli, Z
    Little, MA
    Costigan, D
    Naughten, ER
    Olpin, S
    Muntoni, F
    King, MD
    NEUROPEDIATRICS, 2004, 35 (05) : 312 - 316
12345