A rare case of Crigler–Najjar syndrome type 2: A case report and literature review
Divas Rijal, Prabhat Rijal, Shyam Murti Bohare, Ashish Sanjay Chaudhari, Mandip Dhungel, Mayank Agarwal, Pramish Bhatta, Tulsi Ram Dhakal, Anjali Bishwokarma, Pooja Kafle · 2023
Read A rare case of Crigler–Najjar syndrome type 2: A case report and literature review by Divas Rijal, Prabhat Rijal, Shyam Murti Bohare, Ashish Sanjay Chaudhari, Mandip Dhungel, Mayank Agarwal, Pramish Bhatta, Tulsi Ram Dhakal, Anjali Bishwokarma, Pooja Kafle (2023) in the Tower of Babel, a free online library of public-domain works preserved in clean, searchable text. No sign-up. The full text is served as a plain-text file at a predictable URL, where text is present: https://antarctic-labs.com/tower-of-babel/pmc-10643321.txt.
Description
A peer-reviewed research article from Europe PMC (2023). Key Clinical MessageCrigler–Najjar syndrome type 2 should be suspected in any young patient presenting with isolated indirect hyperbilirubinemia where all other common etiologies have been excluded. It is a relatively benign condition that responds to phenobarbitone.AbstractCrigler–Najjar syndrome (CNS) type 2 is an inborn cause of isolated indirect hyperbilirubinemia characterized by a partial deficiency of the enzyme uridine 5′‐diphosphate‐glucuronosyltransferase (UGT) responsible for bilirubin conjugation.
Catalog record
| CREATOR | Divas Rijal, Prabhat Rijal, Shyam Murti Bohare, Ashish Sanjay Chaudhari, Mandip Dhungel, Mayank Agarwal, Pramish Bhatta, Tulsi Ram Dhakal, Anjali Bishwokarma, Pooja Kafle |
|---|---|
| YEAR | 2023 |
| COLLECTION | PAPERS |
| FORMAT | TXT |
| FILE SIZE | 16 KB |
| VERSION | 1.0 |
| LICENSE | CC BY 4.0 |
| RIGHTS | CC BY |
| SOURCE | Europe PMC |