Facial weakness in NM disease
Anterior horn cell
ALS
SMA
Kennedy disease
Polycranialradiculoneuropathy
Lyme disease
Sarcoidosis
Neoplastic meningitis
Chronic meningitis
GBS
CIDP
Neuromuscular junction
Autoimmune myasthenia gravis
Congenital myasthenia gravis
LEMS
Botulism
Muscle
FSHD
Congenital myopathies
Myotonic muscular dystrophy
Inclusion body myositis
Ocular pharyngeal distal myopathy.
Facial weakness, ptosis, and ophthalmoparesis in the newborn period are common features in severe congenital myopathy and suggest the possibility of centronuclear or nemaline myopathy.