Diagnosis, treatment, and follow-up of Fabry disease in pediatrics

The recommendations presented in this document are based on the most up-to-date evidence available at the time of the search and the judgment of clinical experts. They are expected to support daily clinical practice for the diagnosis, treatment, and follow-up of pediatric patients with FD.

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Publication Details

Journal
Molecular Genetics and Metabolism
Published
2025-12-31
DOI
https://doi.org/10.1016/j.ymgme.2025.109709
Citations
1
Primary Topic
Lysosomal Storage Disorders Research
Type
article
Field-Weighted Citation Impact
1.16
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Diagnosis, treatment, and follow-up of Fabry disease in pediatrics

Kelly Acevedo, Jimena Adriana Cáceres-Mosquera, Adriana Isabel Meza-Martínez, Jorge Armando Rojas-Martínez et al.
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Lysosomal Storage Disorders Research
1.16
article

Diagnosis, treatment, and follow-up of Fabry disease in pediatrics

Kelly Acevedo, Jimena Adriana Cáceres-Mosquera, Adriana Isabel Meza-Martínez, Jorge Armando Rojas-Martínez, Pahola Shirley Atehortúa Baena, Juan Guillermo Cárdenas Aguilera, Clímaco Andres Jiménez-Triana, María Fernanda Reina-Ávila, Ana K. Serrano-Gayubo, Catalina Vélez-Echeverry, Juan Carlos Prieto-Rivera, Richard Baquero-Rodríguez, Leticia ia Belmont-Martínez, P Guarnizo-Zuccardi, Gustavo Cabrera, Juan Politei, Nicolás Rozo Agudelo, Paola Del Rocío Mera-Solarte, Martha Isabel Carrascal-Guzmán, Ana María Zarante-Bahamón, Claudia Ximena Flórez-Rodríguez, Maryuri Liseth Duarte-Amorocho, Fernando Javier Perreta, Charles Marques-Lourenço, Jazmín Sánchez-Gómez, Lilian Reyes-Morales, Guillem Pintos-Morell, Hernán Trimarchi-Jurado, Marco Antonio Olivas-Valdez, Diego Bernardo Ripeau, Liliana María Rubio-Elorza, Isabella Canal-Delgado, Claudia Milena Pérez-Alfonso, Gustavo Adolfo Guerrero-Tinoco
article en
1 citations

Abstract

The recommendations presented in this document are based on the most up-to-date evidence available at the time of the search and the judgment of clinical experts. They are expected to support daily clinical practice for the diagnosis, treatment, and follow-up of pediatric patients with FD.

Molecular Genetics and MetabolismVol. 147(3)
Faculdade de Medicina de São José do Rio Preto (BR), Universidad Tecnológica de Bolívar (CO), University of Cartagena (CO), Mexican Social Security Institute (MX), Universidad Pontificia Bolivariana (CO), Pontificia Universidad Javeriana (CO), Alexander von Humboldt Biological Resources Research Institute (CO), University of Boyaca (CO), Universidad de Antioquia (CO), Military University Nueva Granada (CO), Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia (AR), Diagnostico Maipú (AR), Hospital Universitario de Santander (CO), Hospital de Clínicas "José de San Martín" (AR), Clínica Santa María (CO), Vall d'Hebron Hospital Universitari (ES), Fundación Hospital San Pedro (CO), Institute of Cardiology (CO), Escuela Argentina de Negocios (AR), Secretaría de Salud de Bogotá (CO), Instituto Nacional de Pediatria (MX), Hospital Británico de Buenos Aires (AR), Hospital Universitario San Ignacio (CO), Columbia University (US), Universidad del Valle (CO)
Openalex Percentile: Top 15%
Lysosomal Storage Disorders Research
1.16
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