MULTIPLE ACYL-COA DEHYDROGENASE-DEFICIENCY - A NEONATAL ONSET CASE RESPONSIVE TO TREATMENT

被引：6
|
作者：
VERJEE, ZH [1 ]
SHERWOOD, WG [1 ]
机构：
[1] HOSP SICK CHILDREN,RES INST,TORONTO M5G 1X8,ONTARIO,CANADA
来源：
JOURNAL OF INHERITED METABOLIC DISEASE | 1985年 / 8卷
关键词：
D O I：
10.1007/BF01811497
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：137 / 138
页数：2
相关论文
共 50 条
  • [21] Multiple Acyl-CoA Dehydrogenase Deficiency in an Infant
    Xiao-ming Hu
    Li Li
    The Indian Journal of Pediatrics, 2019, 86 : 194 - 195
  • [22] MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY PRESENTING IN THE NEONATAL-PERIOD - THE FIRST ITALIAN CASE
    BURLINA, AB
    BENNETT, MJ
    GREGERSEN, N
    BARBA, BD
    ZACCHELLO, F
    EUROPEAN JOURNAL OF PEDIATRICS, 1995, 154 (11) : 940 - 941
  • [23] EARLY DIAGNOSIS AND TREATMENT OF NEONATAL MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY - REPORT OF 2 SIBLINGS
    CATZEFLIS, C
    BACHMANN, C
    HALE, DE
    COATES, PM
    WIESMANN, U
    COLOMBO, JP
    JORIS, F
    DELEZE, G
    EUROPEAN JOURNAL OF PEDIATRICS, 1990, 149 (08) : 577 - 581
  • [24] Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency
    Singla, Mohit
    Guzman, Grace
    Griffin, Andrew J.
    Bharati, Saroja
    PEDIATRIC CARDIOLOGY, 2008, 29 (02) : 446 - 451
  • [25] 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
  • [26] 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)
  • [27] Energy utilization issues in multiple acyl-CoA dehydrogenase deficiency type II (severe neonatal onset)
    Bannister, E. N.
    Arduini, K. J.
    MOLECULAR GENETICS AND METABOLISM, 2024, 141 : 29 - 30
  • [28] A novel mutation in ETFDH manifesting as severe neonatal-onset multiple acyl-CoA dehydrogenase deficiency
    van der Westhuizena, Francois H.
    Smuts, Izelle
    Honey, Engela
    Louw, Roan
    Schoonen, Maryke
    Jonck, Lindi-Maryn
    Dercksen, Marli
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2018, 384 : 121 - 125
  • [29] Hyperhomocysteinemia in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
    Zhang, Huiqiu
    Zhao, Rongjuan
    Ma, Jing
    Zhang, Jingfei
    Wang, Juan
    Chang, Xueli
    Guo, Junhong
    Zhang, Wei
    MUSCLE & NERVE, 2023, 68 (05) : 750 - 757
  • [30] 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
12345