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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)

 

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