Holocarboxylase Synthetase Deficiency

Introduction: Holocarboxylase Synthetase Deficiency

Description of Holocarboxylase Synthetase Deficiency

Holocarboxylase Synthetase Deficiency (medical condition): An inherited disorder where the enzymes that use the vitamin...more »

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Holocarboxylase synthetase deficiency:
  »Introduction: Holocarboxylase synthetase deficiency
  »Symptoms of Holocarboxylase synthetase deficiency

Holocarboxylase Synthetase Deficiency: The neonatal form of MULTIPLE CARBOXYLASE DEFICIENCY that is caused by a defect or deficiency in holocarboxylase synthetase. HLCS is the enzyme that covalently links biotin to the biotin dependent carboxylases (propionyl-CoA-carboxylase, pyruvate carboxylase, and beta-methylcrotonyl-CoA carboxylase).
Source: MeSH 2007

Holocarboxylase Synthetase Deficiency: Related Topics

These medical condition or symptom topics may be relevant to medical information for Holocarboxylase Synthetase Deficiency:

• Holocarboxylase Synthetase
• Synthetase
• Deficiency
• Deficiency disease

Holocarboxylase Synthetase Deficiency as a Disease

Holocarboxylase Synthetase Deficiency (medical condition): See Holocarboxylase synthetase deficiency (disease information).
  »Introduction: Holocarboxylase synthetase deficiency
  »Symptoms of Holocarboxylase synthetase deficiency

Holocarboxylase Synthetase Deficiency: Related Diseases

Holocarboxylase Synthetase Deficiency: Holocarboxylase Synthetase Deficiency 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

More information on medical condition: Holocarboxylase synthetase deficiency:

• Information about Holocarboxylase synthetase deficiency
• Basic Summary for Holocarboxylase synthetase deficiency
• Symptoms of Holocarboxylase synthetase deficiency

Holocarboxylase Synthetase Deficiency: Related Disease Topics

These medical disease topics may be related to Holocarboxylase Synthetase Deficiency:

• inherited disorder
• biotin
• seizures
• coma
• delayed development
• alopecia
• lethargy
• dyspnea

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