Kernicterus in a boy with ornithine transcarbamylase deficiency: A case report-Reference-Cited by-同舟云学术

Kernicterus in a boy with ornithine transcarbamylase deficiency: A case report

Published:2017-08-16 Issue:6 Volume:37 Page:586-590
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

López-Corella Eduardo¹,Ibarra-González Isabel²,Fernández-Lainez Cynthia³,Rodríguez-Weber Miguel Á.⁴,Guillén-Lopez Sara³,Belmont-Martínez Leticia³,Agüero-Linares David⁵,Vela-Amieva Marcela³^ORCID

Affiliation:

1. Department of Pathology; National Institute of Pediatrics; Mexico City Mexico State Mexico

2. Nutritional Genetics Unit; Biomedical Research Institute UNAM-National Institute of Pediatrics; Mexico City Mexico State Mexico

3. Inborn Errors of Metabolism and Screening Laboratory; National Institute of Pediatrics; Mexico City Mexico State Mexico

4. Department of Neonatology; National Institute of Pediatrics; Mexico City Mexico State Mexico

5. Valle-Medical Clinic; Ecatepec Mexico State Mexico

Publisher

Wiley

Subject

Clinical Neurology,General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/neup.12404/fullpdf

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5. AAV gene therapy corrects OTC deficiency and prevents liver fibrosis in aged OTC-knock out heterozygous mice;Wang;Mol Genet Metab,2017

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3. Clinicopathological Spectrum of Bilirubin Encephalopathy/Kernicterus;Diagnostics;2019-02-28

4. Acute Presentation and Management of the Encephalopathic Child With an Undiagnosed Inborn Error of Metabolism;The Journal of Emergency Medicine;2019-01

5. Gene Mutation Analysis and Prenatal Diagnosis of the Ornithine Transcarbamylase (OTC) Gene in Two Families with Ornithine Transcarbamylase Deficiency;Medical Science Monitor;2018-10-18