MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex

Introduction: MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex

Description of MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex

MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex (medical condition): A very rare inherited metabolic disorder involving abnormal metabolism...more »

See also:

Maple syrup urine disease, type 1B:
  »Introduction: Maple syrup urine disease, type 1B
  »Symptoms of Maple syrup urine disease, type 1B

MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex: Related Topics

These medical condition or symptom topics may be relevant to medical information for MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex:

• Branched-chain alpha-keto acid dehydrogenase
• Keto acid
• MSUD
• Deficiency
• Deficiency disease
• Subunit
• Chain
• Keto

MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex: Rare Disease

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

MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex, or a subtype of MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex as a Disease

MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex: Another name for Maple syrup urine disease, type 1B (or close medical condition association).
  »Introduction: Maple syrup urine disease, type 1B
  »Symptoms of Maple syrup urine disease, type 1B

MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex: Related Diseases

MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex: MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex 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
• Urinary system conditions

Symptoms of MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex (Maple syrup urine disease, type 1B)

Some of the symptoms of MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex incude:

• Vomiting
• Feeding difficulty
• Failure to thrive
• Absence of grasping reflex
• Irregular breathing

See full list of 21 symptoms of MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex (Maple syrup urine disease, type 1B)

MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex: Related Disease Topics

These medical disease topics may be related to MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex:

• rare inherited metabolic disorder
• branched chain amino acid disorder
• vomiting
• feeding difficulties
• dyspnea

Terms associated with MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex:

Terms Similar to MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex:

• MSUD, type IB
• MSUD, type III (formerly)
• Maple syrup urine disease, type IB

Source - NIH

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