A Rare Cause of Neonatal Hypotonia: First Case of Autosomal Recessive Fast-Channel Congenital Myasthenic Syndrome Type 1B in Albania
Diagnosing a Small Intracranial Subependymal Cyst with a Febrile Epilepsy using Magnetic Resonance Imaging: A Rare Case Report
A Novel SLC9A6 Mutation Associated with Christianson Syndrome in a Non-Consanguineous Iranian Family: A Case Report