LP Ng

Autoimmune glial fibrillary acidic protein astrocytopathy: a case report from Hong Kong

Autoimmune glial fibrillary acidic protein astrocytopathy (GFAP-A) is a rare autoimmune disorder first described in 2016. 1 It typically presents as acute or subacute meningitis, encephalitis, and/ or myelitis, with symptoms such as fever, cognitive decline, limb weakness, and au...