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What is McPherson-Robertson-Cammarano syndrome?

What is McPherson-Robertson-Cammarano syndrome?

  • McPherson-Robertson-Cammarano syndrome: A very rare inherited disorder characterized by droopy eyelids, strabismus and ectopic pupils.

McPherson-Robertson-Cammarano syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that McPherson-Robertson-Cammarano syndrome, or a subtype of McPherson-Robertson-Cammarano syndrome, 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 McPherson-Robertson-Cammarano syndrome as a "rare disease".
Source - Orphanet

McPherson-Robertson-Cammarano syndrome: Introduction

Types of McPherson-Robertson-Cammarano syndrome:

Broader types of McPherson-Robertson-Cammarano syndrome:

What causes McPherson-Robertson-Cammarano syndrome?

Causes of McPherson-Robertson-Cammarano syndrome: see causes of McPherson-Robertson-Cammarano syndrome

What are the symptoms of McPherson-Robertson-Cammarano syndrome?

Symptoms of McPherson-Robertson-Cammarano syndrome: see symptoms of McPherson-Robertson-Cammarano syndrome

McPherson-Robertson-Cammarano syndrome: Testing

Diagnostic testing: see tests for McPherson-Robertson-Cammarano syndrome.

Misdiagnosis: see misdiagnosis and McPherson-Robertson-Cammarano syndrome.

How is it treated?

Doctors and Medical Specialists for McPherson-Robertson-Cammarano syndrome: Medical Geneticist ; see also doctors and medical specialists for McPherson-Robertson-Cammarano syndrome.
Treatments for McPherson-Robertson-Cammarano syndrome: see treatments for McPherson-Robertson-Cammarano syndrome

Name and Aliases of McPherson-Robertson-Cammarano syndrome

Main name of condition: McPherson-Robertson-Cammarano syndrome

Other names or spellings for McPherson-Robertson-Cammarano syndrome:

Dominantly inherited ptosis, strabismus and ectopic pupils

Dominantly inherited ptosis, strabismus and ectopic pupils
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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