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Peters anomaly

Peters anomaly: Introduction

Peters anomaly: A very rare disorder that occurs in the early stages of fetal development and results in infant glaucoma and sometimes other anomalies. More detailed information about the symptoms, causes, and treatments of Peters anomaly is available below.

Symptoms of Peters anomaly

Home Diagnostic Testing

Home medical testing related to Peters anomaly:

Wrongly Diagnosed with Peters anomaly?

Peters anomaly: Related Patient Stories

Peters anomaly: Deaths

Read more about Deaths and Peters anomaly.

Peters anomaly: Complications

Read more about complications of Peters anomaly.

Causes of Peters anomaly

Read more about causes of Peters anomaly.

More information about causes of Peters anomaly:

Peters anomaly: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Peters anomaly: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for Peters anomaly

Medical research articles related to Peters anomaly include:

Click here to find more evidence-based articles on the TRIP Database

Peters anomaly: Animations

Research about Peters anomaly

Visit our research pages for current research about Peters anomaly treatments.

Clinical Trials for Peters anomaly

The US based website lists information on both federally and privately supported clinical trials using human volunteers.

Some of the clinical trials listed on for Peters anomaly include:

Statistics for Peters anomaly

Peters anomaly: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Peters anomaly, or answer someone else's question, on our message boards:

Definitions of Peters anomaly:

Peters anomaly is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Peters anomaly, or a subtype of Peters anomaly, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Peters anomaly as a "rare disease".
Source - Orphanet


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