What is Fountain Syndrome?
What is Fountain Syndrome?
- Fountain Syndrome: A very rare inherited disorder involving mental retardation, sensorineural deafness, skeletal defects, coarse facial features and full lips.
Fountain Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Fountain Syndrome, or a subtype of Fountain 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 Fountain Syndrome as a "rare disease".
Source - Orphanet
Fountain Syndrome: Introduction
Types of Fountain Syndrome:
Broader types of Fountain Syndrome:
What causes Fountain Syndrome?
Causes of Fountain Syndrome: see causes of Fountain Syndrome
What are the symptoms of Fountain Syndrome?
Symptoms of Fountain Syndrome:
see symptoms of Fountain Syndrome
Onset of Fountain Syndrome: birth
Fountain Syndrome: Testing
Diagnostic testing: see tests for Fountain Syndrome.
Misdiagnosis: see misdiagnosis and Fountain Syndrome.
How is it treated?
Doctors and Medical Specialists for Fountain Syndrome: Medical Geneticist
;
see also doctors and medical specialists for Fountain Syndrome.
Treatments for Fountain Syndrome:
see treatments for Fountain Syndrome
Name and Aliases of Fountain Syndrome
Main name of condition: Fountain Syndrome
Other names or spellings for Fountain Syndrome:
mental retardation [sensorineural deafness - skeletal defects - coarse face - full lips]
Mental retardation-deafnes, skeletal abnormalities, coarse face with full lips
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
Fountain Syndrome: Related Conditions
Research the causes of these diseases that are similar to, or related to, Fountain Syndrome: