3 alpha methylcrotonylglycinuria 1

Introduction: 3 alpha methylcrotonylglycinuria 1

Description of 3 alpha methylcrotonylglycinuria 1

3 alpha methylcrotonylglycinuria 1 (medical condition): A rare inherited disorder where lack of a certain enzyme (3...more »

See also:

3 alpha methylcrotonyl-Coa carboxylase 1 deficiency:
  »Introduction: 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency
  »Symptoms of 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency
  »Treatments for 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency

3 alpha methylcrotonylglycinuria 1: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

3 alpha methylcrotonylglycinuria 1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that 3 alpha methylcrotonylglycinuria 1, or a subtype of 3 alpha methylcrotonylglycinuria 1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

3 alpha methylcrotonylglycinuria 1 as a Disease

3 alpha methylcrotonylglycinuria 1: Another name for 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency (or close medical condition association).
  »Introduction: 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency
  »Symptoms of 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency
  »Treatments for 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency

3 alpha methylcrotonylglycinuria 1: Related Diseases

3 alpha methylcrotonylglycinuria 1: 3 alpha methylcrotonylglycinuria 1 is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Metabolic conditions
• Congenital conditions - metabolic disorders
• Congenital conditions

Symptoms of 3 alpha methylcrotonylglycinuria 1 (3 alpha methylcrotonyl-Coa carboxylase 1 deficiency)

Some of the symptoms of 3 alpha methylcrotonylglycinuria 1 incude:

• Feeding difficulties
• Recurring episodes of vomiting
• Recurring episodes of diarrhea
• Lethargy
• Poor muscle tone

See full list of 6 symptoms of 3 alpha methylcrotonylglycinuria 1 (3 alpha methylcrotonyl-Coa carboxylase 1 deficiency)

Treatments for 3 alpha methylcrotonylglycinuria 1 (3 alpha methylcrotonyl-Coa carboxylase 1 deficiency)

Treatments for 3 alpha methylcrotonylglycinuria 1 (3 alpha methylcrotonyl-Coa carboxylase 1 deficiency) include:

• Low-protein diet and supplements

Read more about treatments for 3 alpha methylcrotonylglycinuria 1

Treatment of 3 alpha methylcrotonylglycinuria 1: For more treatment information about 3 alpha methylcrotonylglycinuria 1, see treatment of 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency (3 alpha methylcrotonylglycinuria 1)

3 alpha methylcrotonylglycinuria 1: Related Disease Topics

These medical disease topics may be related to 3 alpha methylcrotonylglycinuria 1:

• rare inherited disorder
• lethargy
• vomiting
• diarrhoea
• hypotonia

Terms associated with 3 alpha methylcrotonylglycinuria 1:

Terms Similar to 3 alpha methylcrotonylglycinuria 1:

• MCC 1 deficiency
• 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency
• 3 Methylcrotonyl-CoA carboxylase deficiency
• 3 Methylcrotonylglycinuria

Source - NIH

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