Literature DB >> 31598103

Inborn Errors of Metabolism in Pediatric Epilepsy.

Anna S Cosnahan, Christopher T Campbell.   

Abstract

Patients with refractory epilepsy from inborn errors of metabolism typically present as neonates. Direct supplementation with the deficient vitamin or cofactor is recommended, and case series report both efficacy and safety data of these agents. Some conditions may also occur together, necessitating multiple treatments. Despite effective and early treatment, patients are at heightened risk for neurological sequela. The literature on seizures related to metabolic deficiencies for pediatric patients is limited but has some guidance on appropriate dosing and monitoring for agents to target specific deficiencies, which may help with narrowing antiepileptic therapies, reducing side effects, and improving neurodevelopmental outcomes and quality of life. The focus of this review is to discuss the pharmacotherapy, including the most updated published efficacy and safety data, involved in treating refractory epilepsy as a result of metabolic errors. Copyright Published by the Pediatric Pharmacy Advocacy Group. All rights reserved. For permissions, email: matthew.helms@ppag.org 2019.

Entities:  

Keywords:  epilepsy; inborn errors of metabolism; neonatal; pediatric

Year:  2019        PMID: 31598103      PMCID: PMC6782122          DOI: 10.5863/1551-6776-24.5.398

Source DB:  PubMed          Journal:  J Pediatr Pharmacol Ther        ISSN: 1551-6776


  35 in total

1.  Long-term outcome in pyridoxine-dependent epilepsy.

Authors:  Levinus A Bok; Feico J Halbertsma; Saskia Houterman; Ron A Wevers; Charlotte Vreeswijk; Cornelis Jakobs; Eduard Struys; Johan H Van Der Hoeven; Deborah A Sival; Michèl A Willemsen
Journal:  Dev Med Child Neurol       Date:  2012-07-13       Impact factor: 5.449

2.  Pyridoxal Phosphate Supplementation in Neuropediatric Disorders.

Authors:  Elisenda Cortès-Saladelafont; Marta Molero-Luis; Rafael Artuch; Àngels García-Cazorla
Journal:  Semin Pediatr Neurol       Date:  2016-11-10       Impact factor: 1.636

3.  Cerebral folate deficiency.

Authors:  Vincent Th Ramaekers; Nenad Blau
Journal:  Dev Med Child Neurol       Date:  2004-12       Impact factor: 5.449

4.  Pyridoxine-dependent seizures: demographic, clinical, MRI and psychometric features, and effect of dose on intelligence quotient.

Authors:  P Baxter; P Griffiths; T Kelly; D Gardner-Medwin
Journal:  Dev Med Child Neurol       Date:  1996-11       Impact factor: 5.449

5.  Pyridoxal phosphate-responsive epilepsy with resistance to pyridoxine.

Authors:  Meng-Fai Kuo; Huei-Shyong Wang
Journal:  Pediatr Neurol       Date:  2002-02       Impact factor: 3.372

6.  Folinic acid-responsive seizures are identical to pyridoxine-dependent epilepsy.

Authors:  Renata C Gallagher; Johan L K Van Hove; Gunter Scharer; Keith Hyland; Barbara Plecko; Paula J Waters; Saadet Mercimek-Mahmutoglu; Sylvia Stockler-Ipsiroglu; Gajja S Salomons; Efraim H Rosenberg; Eduard A Struys; Cornelis Jakobs
Journal:  Ann Neurol       Date:  2009-05       Impact factor: 10.422

7.  Clinical findings in four children with biotinidase deficiency detected through a statewide neonatal screening program.

Authors:  B Wolf; G S Heard; L G Jefferson; V K Proud; W E Nance; K A Weissbecker
Journal:  N Engl J Med       Date:  1985-07-04       Impact factor: 91.245

Review 8.  Pyridoxine-dependent seizures and cognition in adulthood.

Authors:  Kathleen Baynes; Sarah Tomaszewski Farias; Sidney M Gospe
Journal:  Dev Med Child Neurol       Date:  2003-11       Impact factor: 5.449

9.  Technical standards and guidelines for the diagnosis of biotinidase deficiency.

Authors:  Tina M Cowan; Miriam G Blitzer; Barry Wolf
Journal:  Genet Med       Date:  2010-07       Impact factor: 8.822

10.  Vitamin-responsive epileptic encephalopathies in children.

Authors:  Satish Agadi; Michael M Quach; Zulfi Haneef
Journal:  Epilepsy Res Treat       Date:  2013-07-25
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