A Cause of Refractory Seizures: Fumarase Deficiency

被引:0
作者
Yekeduz, Merve Koc [1 ]
Dogulu, Neslihan [1 ]
Oncul, Ummuhan [1 ]
Kose, Engin [1 ]
Unal, Ozlem [2 ]
Eminoglu, Fatma Tuba [1 ]
机构
[1] Ankara Univ, Fac Med, Dept Pediat Metab, Mamak St, TR-06230 Ankara, Turkiye
[2] Kocaeli Univ, Fac Med, Dept Pediat Metab, Kocaeli, Turkiye
关键词
Facial anomalies; fumarase deficiency; hypotonia; seizure; PRENATAL-DIAGNOSIS; ACIDURIA;
D O I
10.4103/jpn.JPN_105_21
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Fumarase is an enzyme involved in the Krebs cycle. Fumarase deficiency (FD) is an autosomal recessive disorder that is associated with neurocognitive dysfunctions. In the absence of fumarase, fumarate is accumulated and excreted in the urine. FD has been reported with polyhydramnios, intrauterine growth retardation, prematurity, hypotonia, seizure, facial anomalies, malnutrition, relative macrocephaly, and developmental retardation. Cranial imaging findings are enlargement of the ventricles, polymicrogyria, and thinning of the corpus callosum. Electroencephalogram findings are generally compatible with hypsarrhythmia. Treatment is generally supportive. Although protein-restricted diets have been tried, their benefits have not been proven. This report aimed to present a case with hypotonia, and refractory seizures were diagnosed at a very early age, and a summary of the cases is found in the literature.
引用
收藏
页码:172 / 176
页数:5
相关论文
共 13 条
[1]   Fumaric aciduria: an overview and the first Brazilian case report [J].
Allegri, Gabriella ;
Fernandes, Marcia J. ;
Scalco, Fernanda B. ;
Correia, Patricia ;
Simoni, Ruth E. ;
Llerena, Juan C., Jr. ;
Costa de Oliveira, Maria L. .
JOURNAL OF INHERITED METABOLIC DISEASE, 2010, 33 (04) :411-419
[2]   A rare cause of opistotonus; fumaric aciduria: The first case presentation in Turkey [J].
Bastug, Osman ;
Kardas, Fatih ;
Ozturk, Mehmet Adnan ;
Halis, Hulya ;
Memur, Seyma ;
Korkmaz, Levent ;
Tag, Zuhal ;
Gunes, Tamer .
TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, 2014, 49 (01) :74-76
[3]   Molecular analysis and prenatal diagnosis of human fumarase deficiency [J].
Coughlin, EM ;
Christensen, E ;
Kunz, PL ;
Krishnamoorthy, KS ;
Walker, V ;
Dennis, NR ;
Chalmers, RA ;
Elpeleg, ON ;
Whelan, D ;
Pollitt, RJ ;
Ramesh, V ;
Mandell, R ;
Shih, VE .
MOLECULAR GENETICS AND METABOLISM, 1998, 63 (04) :254-262
[4]  
Ewbank CKJ., 2006, Gene Review
[5]  
Kerrigan JF, 2000, ANN NEUROL, V47, P583, DOI 10.1002/1531-8249(200005)47:5<583::AID-ANA5>3.0.CO
[6]  
2-Y
[7]   Mild fumarase deficiency and a trial of low protein diet [J].
Kimonis, V. E. ;
Steller, J. ;
Sahai, I. ;
Grange, D. K. ;
Shoemaker, J. ;
Zelaya, B. M. ;
Mandell, R. ;
Shih, K. ;
Shih, V. .
MOLECULAR GENETICS AND METABOLISM, 2012, 107 (1-2) :241-242
[8]   Fumarase deficiency presenting with periventricular cysts [J].
Loeffen, J ;
Smeets, R ;
Voit, T ;
Hoffmann, G ;
Smeitink, J .
JOURNAL OF INHERITED METABOLIC DISEASE, 2005, 28 (05) :799-800
[9]   Detection of a Novel FH Whole Gene Deletion in the Propositus Leading to Subsequent Prenatal Diagnosis in a Sibship With Fumarase Deficiency [J].
Mroch, Amelia R. ;
Laudenschlager, Mark ;
Flanagan, Jason D. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (01) :155-158
[10]   Clinical and Biochemical Heterogeneity Associated with Fumarase Deficiency [J].
Ottolenghi, Chris ;
Hubert, Laurence ;
Allanore, Yannick ;
Brassier, Anais ;
Altuzarra, Cecilia ;
Mellot-Draznieks, Caroline ;
Bekri, Soumeya ;
Goldenberg, Alice ;
Veyrieres, Severine ;
Boddaert, Nathalie ;
Barbier, Valerie ;
Valayannopoulos, Vassili ;
Slama, Abdelhamid ;
Chretien, Dominique ;
Ricquier, Daniel ;
Marret, Stephane ;
Frebourg, Thierry ;
Rabier, Daniel ;
Munnich, Arnold ;
de Keyzer, Yves ;
Toulhoat, Herve ;
de Lonlay, Pascale .
HUMAN MUTATION, 2011, 32 (09) :1046-1052