What is Pierson syndrome?
What is Pierson syndrome?
- Pierson syndrome: A very rare syndrome characterized mainly by a small pupil and kidney disease at birth.
Pierson syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Pierson syndrome, or a subtype of Pierson 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 Pierson syndrome as a "rare disease".
Source - Orphanet
Pierson syndrome: Introduction
Types of Pierson syndrome:
Broader types of Pierson syndrome:
What causes Pierson syndrome?
Causes of Pierson syndrome: see causes of Pierson syndrome
What are the symptoms of Pierson syndrome?
Symptoms of Pierson syndrome:
see symptoms of Pierson syndrome
Pierson syndrome: Testing
Diagnostic testing: see tests for Pierson syndrome.
Misdiagnosis: see misdiagnosis and Pierson syndrome.
How is it treated?
Doctors and Medical Specialists for Pierson syndrome: Medical Geneticist
;
see also doctors and medical specialists for Pierson syndrome.
Treatments for Pierson syndrome:
see treatments for Pierson syndrome
Research for Pierson syndrome:
see research for Pierson syndrome
Name and Aliases of Pierson syndrome
Main name of condition: Pierson syndrome
Other names or spellings for Pierson syndrome:
microcoria [congenital nephrosis], Microcoria and congenital nephrotic syndrome
Microcoria and congenital nephrotic syndrome
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)