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Crigler Najjar syndrome

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Disease classification WHO
E 80.5 Crigler Najjar Syndrome

Crigler Najjar syndrome[1] is a rare inherited disorder affecting the metabolism of bilirubin, a chemical formed from the breakdown of the heme in red blood cells [2]


Najjar was a libanese paediatrician [3]

John Fiedling Crigler [4] [5]