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)