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Aspartylglucosaminidase deficiency

Aspartylglucosaminidase deficiency: Introduction

Aspartylglucosaminidase deficiency: 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 Aspartylglucosaminidase deficiency is available below.

Symptoms of Aspartylglucosaminidase deficiency

See full list of 37 symptoms of Aspartylglucosaminidase deficiency

Aspartylglucosaminidase deficiency: Complications

Review possible medical complications related to Aspartylglucosaminidase deficiency:

Wrongly Diagnosed with Aspartylglucosaminidase deficiency?

Causes of Aspartylglucosaminidase deficiency

Read more about causes of Aspartylglucosaminidase deficiency.

Treatments for Aspartylglucosaminidase deficiency

  • 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 Aspartylglucosaminidase deficiency

Prognosis for Aspartylglucosaminidase deficiency

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

More about prognosis of Aspartylglucosaminidase deficiency

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