Alpers’ Huttenlocher Disease

Alpers’ Huttenlocher Disease

Article
Brain & Nerve
Eye & Vision
+4
Contributed byKrish Tangella MD, MBAMar 17, 2018

The topic Alpers’ Huttenlocher Disease you are seeking is a synonym, or alternative name, or is closely related to the medical condition Alpers’ Disease.

Quick Summary:

  • Alpers’ Disease is a neurodevelopmental genetic disorder that is characterized by the loss of grey matter in the brain (grey matter is a major component of the brain)
  • It is caused by mutations in the POLG polymerase gene, which codes for the production of mitochondrial DNA
  • Even though the disorder is inherited and present at the time of birth, symptoms may take weeks to years to develop. Once symptoms have arisen, they rapidly become worse
  • The three primary symptoms of Alpers’ Disease are dementia, seizure disorder, and liver disease
  • Currently, there is no cure for the disease and no way to slow progression of the symptoms. But through medications, some of the symptoms may be eased

Please find comprehensive information on Alpers’ Disease regarding definition, distribution, risk factors, causes, signs & symptoms, diagnosis, complications, treatment, prevention, prognosis, and additional useful information HERE.

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Krish Tangella MD, MBA

Pathology, Medical Editorial Board, DoveMed Team

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