There are many criteria that can help in the proper general diagnosis of alternating hemiplegia.

There is no diagnostic test for alternating hemiplegia, which makes it very difficult to diagnose.

Many children affected by alternating hemiplegia also suffer from epilepsy.

This gene is the likely genetic cause of alternating hemiplegia of childhood.

While Flunarizine does not stop the attacks, it is most common drug prescribed to treat those suffering from alternating hemiplegia.

Weber's syndrome is the only form of alternating hemiplegia that is somewhat easy to diagnose beyond the general criteria.

Also, because alternating hemiplegia is extremely rare, it is frequently missed and the patient is often misdiagnosed.

It may help to reduce the severity and duration of attacks of paralysis associated with the more serious form of alternating hemiplegia.

Some common symptoms of alternating hemiplegia are mental impairment, gait and balance difficulties, excessive sweating and changes in body temperature.

Alternating hemiplegia refers to a form of hemiplegia that has an ipsilateral and contralateral presentation in different parts of the body.

In a study of fifteen females and nine males' patient with alternating hemiplegia, a mutation in ATP1A3 gene was present.

Mutations in the ATP1A2 gene has been implicated in the familial form of alternating hemiplegia of childhood.

Weber's syndrome (superior alternating hemiplegia) is a form of stroke characterized by the presence of an oculomotor nerve palsy and contralateral hemiparesis or hemiplegia.

This occurrence is very indicative of alternating hemiplegia and as such those who display this are usually diagnosed with probable alternating hemiplegia.

FHM can also present with the same signs as benign familial infantile convulsions (BFIC) and alternating hemiplegia of childhood.

Those suffering from alternating hemiplegia are often underweight and with the help of dietitians, a meal plan should be developed for times of attack when consumption of food may be difficult.

There is clinical overlap in some FHM patients with episodic ataxia type 2 and spinocerebellar ataxia type 6, benign familial infantile epilepsy, and alternating hemiplegia of childhood.

Weber's syndrome (also known as superior alternating hemiplegia) has a few distinct symptoms: contralateral hemiparesis of limb and facial muscle accompanied by weakness in one or more muscles that control eye movement on the same side.

Alternating hemiplegia of childhood (AHC) is a rare neurological disorder of uncertain etiology, though growing evidence strongly supports mutation of the ATP1A3 gene as the primary cause of this disease.

There are multiple forms of alternating hemiplegia, Weber's syndrome, Middle Alternating Hemiplegia, and Inferior Alternating Hemiplegia.

Although common, the paroxysmal disorders involving the eye, nystagmus and strabismus, may not be apparent in older children and may not have been remembered in childhood so a lack of these symptoms does not rule out alternating hemiplegia.

Inferior Alternating Hemiplegia (also known as medial medullary syndrome) typically involves a "weakness of the extremities accompanied by paralysis of muscles on the ipsilateral side of the tongue (seen as a deviation of the tongue on that side on protrusion).

AHC Alternating Hemiplegia Syndrome None Alternating hemiplegia of childhood (AHC) is a rare neurological disorder characterized by frequent, temporary episodes of paralysis on one side of the body (hemiplegia).

Medial medullary syndrome, also known as inferior alternating syndrome, hypoglossal alternating hemiplegia, lower alternating hemiplegia, or Dejerine syndrome, is a type of alternating hemiplegia characterized by a set of clinical features resulting from occlusion of the anterior spinal artery.