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Diseases » Aspartylglycosaminuria » Introduction
 

Aspartylglycosaminuria

Aspartylglycosaminuria: Introduction

Aspartylglycosaminuria: A rare glycoprotein metabolism disorder caused by a deficiency of an enzyme called aspartylglucosaminidase. Patients tend to develop normally during the first few years of life and development continues slowly until adolescence when mental retardation becomes progressively worse. More detailed information about the symptoms, causes, and treatments of Aspartylglycosaminuria is available below.

Symptoms of Aspartylglycosaminuria

See full list of 40 symptoms of Aspartylglycosaminuria

Aspartylglycosaminuria: Complications

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Disease Topics Related To Aspartylglycosaminuria

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Wrongly Diagnosed with Aspartylglycosaminuria?

Causes of Aspartylglycosaminuria

Read more about causes of Aspartylglycosaminuria.

Treatments for Aspartylglycosaminuria

  • There is no cure and no definitive treatment. Allogenic bone marrow grafts have not proved to be particularly helpful. Symptomatic measures such as anti-seizure medication may be used if seizures develop
  • more treatments...»

Read more about treatments for Aspartylglycosaminuria

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Prognosis for Aspartylglycosaminuria

Prognosis for Aspartylglycosaminuria: Patients tend to survive until mid-adulthood. Mental retardation and disability may be severe by this stage.

More about prognosis of Aspartylglycosaminuria

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Definitions of Aspartylglycosaminuria:

Aspartylglycosaminuria is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Aspartylglycosaminuria, or a subtype of Aspartylglycosaminuria, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)


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