Recommendations for Infantile-Onset and Late-Onset Pompe Disease: An Iranian Consensus

Background: Pompe disease, also denoted as acid maltase or acid α-glucosidase deficiency or glycogen storage disease type II, is a rare, autosomal recessive lysosomal storage disorder. Several reports have previously described Pompe disease in Iran and considering increased awareness of related subs...

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Detalles Bibliográficos
Autores principales: Fatehi, Farzad, Ashrafi, Mahmoud Reza, Babaee, Marzieh, Ansari, Behnaz, Beiraghi Toosi, Mehran, Boostani, Reza, Eshraghi, Peyman, Fakharian, Atefeh, Hadipour, Zahra, Haghi Ashtiani, Bahram, Moravej, Hossein, Nilipour, Yalda, Sarraf, Payam, Sayadpour Zanjani, Keyhan, Nafissi, Shahriar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8490649/
https://www.ncbi.nlm.nih.gov/pubmed/34621239
http://dx.doi.org/10.3389/fneur.2021.739931

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