Atrophia Areata

Atrophia Areata

Article
Eye & Vision
Diseases & Conditions
+2
Contributed byKrish Tangella MD, MBAAug 29, 2023

The topic Atrophia Areata you are seeking is a synonym, or alternative name, or is closely related to the medical condition Helicoidal Peripapillary Chorioretinal Degeneration.

Quick Summary:

  • Helicoidal Peripapillary Chorioretinal Degeneration is an extremely rare inherited disorder that affects the choroid and retina, which are parts of the eye. It is classified as a type of choroidal dystrophy
  • Even though it is a congenital condition, the onset of signs and symptoms may occur during childhood or into adulthood
  • The cause of Helicoidal Peripapillary Chorioretinal Degeneration is a genetic mutation that leads to atrophy of the eye parts. Since, the condition is inherited in an autosomal dominant manner; a positive family history is a key risk factor. It is occasionally associated with another genetic disorder abetalipoproteinemia
  • Helicoidal Peripapillary Chorioretinal Degeneration results in signs and symptoms that include presence of blind spots and loss of central vision. The condition is progressive and can result in vision impairment
  • A healthcare provider can use various physical (eye) exams, blood tests, and imaging studies to diagnose Helicoidal Peripapillary Chorioretinal Degeneration
  • Currently, there is no specific treatment available to manage the condition. The prognosis of Helicoidal Peripapillary Chorioretinal Degeneration is typically guarded

Please find comprehensive information on Helicoidal Peripapillary Chorioretinal Degeneration 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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