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3Methylcrotonyl 3Methylcronyl COA Carboxylase (3MCC) Deficiency Care Plan (last updated 2/21/09) Clinical Considerations Most asymptomatic Maternal 3MCC Initial labs (diagnostic & baseline) Diet considerations/
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Who Needs 3-Methylcronyl CoA Carboxylase 3-MCC:
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Individuals diagnosed with 3-Methylcronyl CoA Carboxylase 3-MCC deficiency.
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This genetic disorder affects the body's ability to metabolize certain proteins, resulting in the buildup of harmful substances.
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Newborns who undergo newborn screening for metabolic disorders.
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3-Methylcronyl CoA Carboxylase 3-MCC is one of the disorders tested for in many newborn screening programs worldwide.
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Detecting this condition early allows for timely intervention and management.
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Remember, it's important to consult with a healthcare professional or genetic counselor for specific guidance and advice regarding 3-Methylcronyl CoA Carboxylase 3-MCC and its management.
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What is 3-methylcronyl coa carboxylase 3-mcc?
3-methylcronyl coa carboxylase (3-MCC) is an enzyme involved in the breakdown of certain amino acids and fatty acids in the body.
Who is required to file 3-methylcronyl coa carboxylase 3-mcc?
Medical professionals or laboratories performing tests related to 3-MCC may be required to report results.
How to fill out 3-methylcronyl coa carboxylase 3-mcc?
Fill out the necessary forms provided by the relevant authorities with accurate and complete information.
What is the purpose of 3-methylcronyl coa carboxylase 3-mcc?
The purpose of reporting 3-MCC levels is to monitor and diagnose certain genetic disorders related to amino acid metabolism.
What information must be reported on 3-methylcronyl coa carboxylase 3-mcc?
The test results indicating the levels of 3-MCC in the patient's blood or urine.
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