Wikisage, the free encyclopedia of the second generation, is digital heritage
Crigler Najjar syndrome: Difference between revisions
Jump to navigation
Jump to search
mNo edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
{{disease|E 80.5|Crigler Najjar Syndrome}} | {{disease|E 80.5|Crigler Najjar Syndrome}} | ||
Crigler Najjar syndrome<ref>Pschyrembel Klinisches | Crigler Najjar syndrome<ref>Pschyrembel Klinisches Wörterbuch. de Gruyter 256.Auflage ISBN 3-11-010881-X </ref> | ||
is a rare inherited disorder affecting the metabolism of bilirubin, a chemical formed from the breakdown of the heme in red blood cells | is a rare inherited disorder affecting the metabolism of bilirubin, a chemical formed from the breakdown of the heme in red blood cells | ||
<ref>https://en.wikipedia.org/wiki/Crigler%E2%80%93Najjar_syndrome</ref> | <ref>[https://en.wikipedia.org/wiki/Crigler%E2%80%93Najjar_syndrome wikipedia]</ref> | ||
==Links== | ==Links== | ||
[[Victor_Assad_Najjar|Najjar]] was a libanese paediatrician <ref>http://www.whonamedit.com/doctor.cfm/61.html</ref> | [[Victor_Assad_Najjar|Najjar]] was a libanese paediatrician <ref>http://www.whonamedit.com/doctor.cfm/61.html</ref> | ||
Revision as of 15:17, 5 July 2019
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]
Links
Najjar was a libanese paediatrician [3]
| References: |
|