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Crigler-Najjar Syndrome
Crigler-Najjar Syndrome
Source
Crigler-Najjar syndrome is an inherited disorder in which bilirubin (a substance made by the liver) cannot be changed into its water-soluble form, bilirubin glucuronide. This causes jaundice (yellow… More »
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Crigler-Najjar syndrome - Information from NIH
Alternate Name(s): Glucuronyl transferase deficiency (type I Crigler-Najjar); Arias syndrome (type II Crigler-Najjar) ... Crigler-Najjar syndrome is an inherited disorder in which bilirubin (a substance made by the liver) cannot be changed into its water-soluble form, bilirubin glucuronide. This causes jaundice (yellow discoloration of skin and eyes) and organ ...
70k - 10 sec @ 56k
www.nlm.nih.gov/medlineplus/ency/article/001127.htm#Def... www.nlm.nih.gov/medlineplus/ency/article/001127.htm#Definition
Crigler-Najjar syndrome - Wikipedia, the free encyclopedia
Source
Crigler-Najjar Syndrome or CNS is a rare disorder affecting the metabolism of bilirubin, a chemical formed from the breakdown of blood. The disorder results in an inherited form of non-hemolytic ja...
en.wikipedia.org/wiki/Crigler-Najjar_syndrome
Questions about Crigler-Najjar Syndrome
What is the Crigler-Najjar Syndrome?
What causes Crigler-Najjar syndrome Health Article?
What is Crigler Najjar syndrome type II?
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Crigler-Najjar Syndrome: eMedicine Gastroenterology
Overview: Crigler-Najjar syndrome (CNS) is a rare autosomal recessive disorder of bilirubin metabolism. Two distinct forms have been described, as follows: type 1 and type 2. Type 1 Crigler-Najjar syndrome, first described in 1952 by Crigler and ... ... Crigler-Najjar syndrome is a much rarer disorder, with only a few...
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emedicine.medscape.com/article/172858-overview · Cached
Crigler-Najjar Syndrome
Article describes Crigler-Najjar syndrome, its symptoms, diagnosis, and treatment. ... Crigler-Najjar syndrome is an inherited disorder of bilirubin metabolism. It is an autosomal recessive disorder, meaning that an individual needs to receive two copies of the defective gene, one from each parent, in order to develop...
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rarediseases.about.com/od/rarediseasesc/a/021305.htm
Crigler-Najjar syndrome (www.whonamedit.com)
Crigler-Najjar syndrome: A familial form of congenital hyperbilirubinemia associated with severe disorders of the central nervous system and resembling kernicterus (degeneration of the basal ganglia). Also known as: Arias’ syndrome. ... Hyperbilirubinaemia in newborn in Crigler-Najjar syndrome is called Najjar-Crigler icterus.
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www.whonamedit.com/synd.cfm/86.html · Cached
Crigler-Najjar syndrome - Overview
Crigler-Najjar syndrome - Overview, Crigler-Najjar syndrome is a very rare inherited d... ... Crigler-Najjar syndrome is caused by an abnormal gene. The gene fails to make the enzyme that normally converts bilirubin into a form that can easily be removed from the body.
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www.umm.edu/ency/article/001127.htm · Cached
Crigler-Najjar Syndrome - WrongDiagnosis.com
Crigler-Najjar Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis. ... Symptoms of Crigler-Najjar Syndrome...
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www.wrongdiagnosis.com/c/crigler_najjar_syndrome/intro.... www.wrongdiagnosis.com/c/crigler_najjar_syndrome/intro.htm
Signs of Crigler-Najjar syndrome, type 2 - WrongDiagnosis.com
Signs of Crigler-Najjar syndrome, type 2 including medical signs and symptoms of Crigler-Najjar syndrome, type 2, symptoms, common medical issues, duration, and the correct diagnosis for Crigler-Najjar syndrome, type 2 signs or Crigler-Najjar syndrome, type 2 symptoms. ... Symptoms of Crigler-Najjar syndrome, type 2...
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www.wrongdiagnosis.com/c/crigler_najjar_syndrome_type_2... www.wrongdiagnosis.com/c/crigler_najjar_syndrome_type_2/signs.htm
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