CPEO disease CPEO is an acronym for chronic progressive external ophthalmoplegia and CPEO is also called progressive external ophthalmoplegia (PEO), is a inherited mitochondrial disorder

What is Tolosa Hunt syndrome Tolosa-Hunt syndrome is described as severe and unilateral periorbital headache associated with painful and restricted eye movements ((Amrutkar C, Burton

Miller Fisher syndrome Miller Fisher syndrome also called Fisher’s syndrome, is a rare acquired nerve disease considered to be a rare variant of of Guillain-Barré syndrome

Kearns Sayre syndrome Kearns-Sayre syndrome (KSS) is a very rare multisystem mitochondrial disease defined by 3 primary findings of onset before age 20 years, atypical

POLG POLG also called POLG-related disorders is a group of mitochondrial genetic diseases caused by mutations in the polymerase gamma (pol γ) or PolG gene that have

Kennedy’s disease Kennedy's syndrome also known as Kennedy's disease, X-linked spinal and bulbar muscular atrophy, X-linked spinobulbar muscular atrophy or Spinal and Bulbar Muscular Atrophy (SBMA),

Hand tremors Tremor is a type of rhythmic shaking movement that you can't control that is commonly caused by a neurological condition or a nervous

Potter’s syndrome Potter's syndrome also known as Potter syndrome, Potter sequence or oligohydramnios sequence, is a rare congenital disorder caused by kidney problems and too

PPROM Preterm premature rupture of membranes or PPROM is also known as preterm PROM, is a condition which occurs in pregnancy when the amniotic sac

Joubert syndrome Joubert syndrome, also called familial aplasia of the vermis, molar tooth midbrain-hindbrain malformation, agenesis of cerebellar vermis or cerebello-oculo-renal syndrome, is a rare autosomal