Thelansis

Myasthenia Gravis (MG) is an autoimmune disease characterized by muscle weakness and fatigue. It is a B-cell mediated condition, with antibodies targeting the acetylcholine receptor, muscle-specific kinase (MUSK), lipoprotein-related protein 4 (LRP4), or the postsynaptic membrane at the neuromuscular junction. Auto-antibodies against the acetylcholine receptor (AChR), muscle-specific kinase, and lipoprotein-related protein four are well-established diagnostic markers and pathogenic factors. These auto-antibodies play a crucial role in classifying Myasthenia Gravis patients into subgroups. Fortunately, modern treatments offer a positive prognosis for MG patients, including immunosuppression, symptom management, and support. Most individuals with mild to moderate symptoms achieve complete remission or significant improvement. MG can be categorized into five types: congenital myasthenia gravis, generalized myasthenia gravis, ocular myasthenia gravis, transient neonatal myasthenia gravis, ...