Acidemia glutárica tipo 1: presentación de un caso y revisión de la literatura

作者: Edwin Forero-Sánchez , Olga Yaneth Echeverri-Peña , Eugenia Espinosa-García , Johana María Guevara-Morales , Luis Alejandro Barrera-Avellaneda

DOI: 10.17533/UDEA.IATREIA.V28N2A09

关键词:

摘要: A Acidemia Glutarica tipo-1 e um dos erros inatos do metabolismo diagnosticados com maior frequencia na Colombia. E consequencia de uma alteracao no metabolismo aminoacidos lisina, hidroxilisina e triptofano, da que resulta acumulacao acidos glutarico 3-hidroxiglutarico nos fluidos corporais. Clinicamente transtorno neurologico caracterizado por macrocefalia, atrofia cerebral progressiva e distonia. Por sua evolucao cronica doenca subdiagnosticada, de tal forma podem passar varios anos ate a sintomatologia ou as neuroimagens sugerem etiologia metabolica. No entanto, alguns pacientes apresentam aguda usualmente desencadeada por infeccao entre os 6 18 meses idade. ser susceptivel manejo nutricional, necessario fazer cedo o diagnostico iniciar tratamento, para prevenir melhorar complicacoes doencas intercorrentes. importância considerar AG-1 no diferencial paralisia espastica disquinetica sem historia clara eventos hipoxicos, bem como em regressao nas metas do neurodesenvolvimento. Descreve-se caso apresentacao aguda, ilustra curso clinico enfoque doenca.

参考文章(9)
Jean-Marie Saudubray, S. Kölker, Glutaryl-Coenzyme A dehydrogenase deficiency ,(2003)
J Brismar, P T Ozand, CT and MR of the brain in glutaric acidemia type I: a review of 59 published cases and a report of 5 new patients. American Journal of Neuroradiology. ,vol. 16, pp. 675- 683 ,(1995)
Ma Luz Couce, Olalla López-Suárez, Ma Dolores Bóveda, Daisy E. Castiñeiras, José A. Cocho, Judith García-Villoria, Manuel Castro-Gago, José Ma Fraga, Antonia Ribes, Glutaric aciduria type I: outcome of patients with early- versus late-diagnosis. European Journal of Paediatric Neurology. ,vol. 17, pp. 383- 389 ,(2013) , 10.1016/J.EJPN.2013.01.003
Chee-Seng Lee, Yin-Hsiu Chien, Shinn-Forng Peng, Pin-Wen Cheng, Lih-Maan Chang, Ai-Chu Huang, Wuh-Liang Hwu, Ni-Chung Lee, Promising outcomes in glutaric aciduria type I patients detected by newborn screening Metabolic Brain Disease. ,vol. 28, pp. 61- 67 ,(2013) , 10.1007/S11011-012-9349-Z
Paris Jafari, Olivier Braissant, Luisa Bonafé, Diana Ballhausen, The unsolved puzzle of neuropathogenesis in glutaric aciduria type I Molecular Genetics and Metabolism. ,vol. 104, pp. 425- 437 ,(2011) , 10.1016/J.YMGME.2011.08.027
Krista Viau, Sharon L. Ernst, Rena J. Vanzo, Lorenzo D. Botto, Marzia Pasquali, Nicola Longo, Glutaric acidemia Type 1: Outcomes before and after expanded newborn screening Molecular Genetics and Metabolism. ,vol. 106, pp. 430- 438 ,(2012) , 10.1016/J.YMGME.2012.05.024
Georg F. Hoffmann, Peter Burgard, Stefan Kölker, Ernst Christensen, James V. Leonard, Cheryl R. Greenberg, Avihu Boneh, Alberto B. Burlina, Alessandro P. Burlina, Marjorie Dixon, Marinus Duran, Angels García Cazorla, Stephen I. Goodman, David M. Koeller, Mårten Kyllerman, Chris Mühlhausen, Edith Müller, Jürgen G. Okun, Bridget Wilcken, Diagnosis and management of glutaric aciduria type I - revised recommendations Journal of Inherited Metabolic Disease. ,vol. 34, pp. 677- 694 ,(2011) , 10.1007/S10545-011-9289-5
Chin-Tung Hsieh, Wuh-Liang Hwu, Yuan-Te Huang, Ai-Chu Huang, Shiao-Fang Wang, Min-Huei Hu, Yin-Hsiu Chien, Early Detection of Glutaric Aciduria Type I by Newborn Screening in Taiwan Journal of the Formosan Medical Association. ,vol. 107, pp. 139- 144 ,(2008) , 10.1016/S0929-6646(08)60127-8
Gary L. Hedlund, Nicola Longo, Marzia Pasquali, Glutaric acidemia type 1 American Journal of Medical Genetics Part C: Seminars in Medical Genetics. ,vol. 142C, pp. 86- 94 ,(2006) , 10.1002/AJMG.C.30088