GM2-Gangliosidosis (Sandhoff and Tay Sachs disease): Diagnosis and Neuroimaging Findings (An Iranian Pediatric Case Series)

OBJECTIVE: GM2-Gangliosidosis disease is a rare autosomal recessive genetic disorder that includes two disorders (Tay–Sachs and Sandhoff disease).These disorders cause a progressive deterioration of nerve cells and inherited deficiency in creating hexosaminidases A, B, and AB. MATERIALS & METHOD...

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Detalles Bibliográficos
Autores principales: KARIMZADEH, Parvaneh, JAFARI, Narjes, NEJAD BIGLARI, Habibeh, JABBEH DARI, Sayena, AHMAD ABADI, Farzad, ALAEE, Mohammad-Reza, NEMATI, Hamid, SAKET, Sasan, TONEKABONI, Seyed Hasan, TAGHDIRI, Mohammad-Mahdi, GHOFRANI, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shahid Beheshti University of Medical Sciences 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135282/
https://www.ncbi.nlm.nih.gov/pubmed/25143775

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135282/
https://www.ncbi.nlm.nih.gov/pubmed/25143775

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