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AddressographGlutaric Academia Type 1 (GA1) (New Diagnosis) Care Plan Use in conjunction with Medical Guidelines for management of Metabolic Disorders for required investigation. Problem: Knowledge
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Glutaric aciduria type 1 is a rare genetic disorder that primarily affects infants and young children. Individuals who have a family history of the condition or are experiencing symptoms associated with glutaric aciduria type 1 may need to be tested for this disorder. Additionally, newborn screening programs often include glutaric aciduria type 1 testing to identify affected infants early on. It is crucial to diagnose and manage this condition as early as possible to prevent or minimize long-term complications.
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Glutaric aciduria type 1 is a rare genetic disorder that affects the body's ability to break down certain amino acids.
Glutaric aciduria type 1 must be reported by healthcare providers and genetic counselors.
Glutaric aciduria type 1 can be filled out by providing information about the patient's medical history, symptoms, and genetic testing results.
The purpose of glutaric aciduria type 1 is to track and monitor individuals with the condition for treatment and research purposes.
Information such as patient's name, date of birth, medical history, symptoms, genetic testing results, and treatment plan must be reported on glutaric aciduria type 1.
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