What is Sialuria, Finnish type?
What is Sialuria, Finnish type?
- Sialuria, Finnish type: A rare inherited biochemical disorder characterized by the accumulation of sialic acid in the tissues and excretion of sialic acid in the urine. This condition is an adult form of sialuria.
Sialuria, Finnish type is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Sialuria, Finnish type, or a subtype of Sialuria, Finnish type,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Sialuria, Finnish type: Introduction
Types of Sialuria, Finnish type:
Broader types of Sialuria, Finnish type:
Who gets Sialuria, Finnish type?
Racial predominance for Sialuria, Finnish type:
Most commonly found in Finland
How serious is Sialuria, Finnish type?
Prognosis of Sialuria, Finnish type: A relatively normal life span can be expected.
Complications of Sialuria, Finnish type:
see complications of Sialuria, Finnish type
What causes Sialuria, Finnish type?
Causes of Sialuria, Finnish type: see causes of Sialuria, Finnish type
What are the symptoms of Sialuria, Finnish type?
Symptoms of Sialuria, Finnish type:
see symptoms of Sialuria, Finnish type
Complications of Sialuria, Finnish type:
see complications of Sialuria, Finnish type
Onset of Sialuria, Finnish type: 6-9 months
Can anyone else get Sialuria, Finnish type?
Inheritance:
see inheritance of Sialuria, Finnish type
Sialuria, Finnish type: Testing
Diagnostic testing: see tests for Sialuria, Finnish type.
Misdiagnosis: see misdiagnosis and Sialuria, Finnish type.
How is it treated?
Doctors and Medical Specialists for Sialuria, Finnish type: Medical Geneticist
;
see also doctors and medical specialists for Sialuria, Finnish type.
Treatments for Sialuria, Finnish type:
see treatments for Sialuria, Finnish type
Name and Aliases of Sialuria, Finnish type
Main name of condition: Sialuria, Finnish type
Other names or spellings for Sialuria, Finnish type:
Salla disease
Salla disease, Free sialic acid storage disease, Infantile sialic acid storage disorder (ISSD), N-acetylneuraminic acid (NANA) storage disease (NSD), Sialic acid storage disease
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)