Congenital familial nonhemolytic jaundice

Introduction: Congenital familial nonhemolytic jaundice

Description of Congenital familial nonhemolytic jaundice

Congenital familial nonhemolytic jaundice (medical condition): A rare congenital condition involving a total absence of the liver enzyme called glucoronyl transferase which is needed to change bilirubin into a form that can be removed from the body. The bilirubin builds up in the body and causes damage and severe symptoms.

See also:

Crigler-Najjar syndrome, type 1:
  »Introduction: Crigler-Najjar syndrome, type 1
  »Symptoms of Crigler-Najjar syndrome, type 1

Congenital familial nonhemolytic jaundice: Related Topics

These medical condition or symptom topics may be relevant to medical information for Congenital familial nonhemolytic jaundice:

• Familial nonhemolytic jaundice
• Congenital
• Congenital disease
• Congenital disorder
• Familial
• Familial disorder
• Jaundice (774 causes)
• Jaundice symptoms (693 causes)

Congenital familial nonhemolytic jaundice as a Disease

Congenital familial nonhemolytic jaundice: Another name for Crigler-Najjar syndrome, type 1 (or close medical condition association).
  »Introduction: Crigler-Najjar syndrome, type 1
  »Symptoms of Crigler-Najjar syndrome, type 1

Symptoms of Congenital familial nonhemolytic jaundice (Crigler-Najjar syndrome, type 1)

Some of the symptoms of Congenital familial nonhemolytic jaundice incude:

• Severe jaundice
• Severe central nervous system disorders
• Recurrent fever
• Complete lack of glucoronyl transferase
• High blood bilirubin level

See full list of 9 symptoms of Congenital familial nonhemolytic jaundice (Crigler-Najjar syndrome, type 1)

Congenital familial nonhemolytic jaundice: Related Disease Topics

These medical disease topics may be related to Congenital familial nonhemolytic jaundice:

• hemolytic jaundice
• Rotor syndrome
• Dubin-Johnson syndrome
• Arias syndrome
• jaundice
• photherapy

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Medical dictionaries:

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Jakob's disease

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