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What is Arginine-glycine amidinotransferase deficiency?

What is Arginine-glycine amidinotransferase deficiency?

  • Arginine-glycine amidinotransferase deficiency: A rare enzyme deficiency which manifests as mental retardation, developmental delay and speech problemss.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Arginine-glycine amidinotransferase deficiency as a "rare disease".
Source - Orphanet

Arginine-glycine amidinotransferase deficiency: Introduction

Types of Arginine-glycine amidinotransferase deficiency:

Broader types of Arginine-glycine amidinotransferase deficiency:

What causes Arginine-glycine amidinotransferase deficiency?

Causes of Arginine-glycine amidinotransferase deficiency: see causes of Arginine-glycine amidinotransferase deficiency

What are the symptoms of Arginine-glycine amidinotransferase deficiency?

Symptoms of Arginine-glycine amidinotransferase deficiency: see symptoms of Arginine-glycine amidinotransferase deficiency

Onset of Arginine-glycine amidinotransferase deficiency: infancy

Arginine-glycine amidinotransferase deficiency: Testing

Misdiagnosis: see misdiagnosis and Arginine-glycine amidinotransferase deficiency.

How is it treated?

Doctors and Medical Specialists for Arginine-glycine amidinotransferase deficiency: Medical Geneticist ; see also doctors and medical specialists for Arginine-glycine amidinotransferase deficiency.
Treatments for Arginine-glycine amidinotransferase deficiency: see treatments for Arginine-glycine amidinotransferase deficiency

Name of Arginine-glycine amidinotransferase deficiency

Main name of condition: Arginine-glycine amidinotransferase deficiency

 

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