Hereditary pancreatitis of 3 Chinese children: Case report and literature review

BACKGROUND: Hereditary pancreatitis (HP) is quite rare and is distinguished by incomplete penetrance presentation as early-onset relapsing pancreatitis, usually beginning in childhood. HP is now known to be commonly relevant to mutations in the PRSS1 (gene-encoding cationic trypsinogen), SPINK1 (ser...

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Detalles Bibliográficos
Autores principales: Dai, Li-Na, Chen, Ying-Wei, Yan, Wei-Hui, Lu, Li-Na, Tao, Yi-Jing, Cai, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023873/
https://www.ncbi.nlm.nih.gov/pubmed/27603351
http://dx.doi.org/10.1097/MD.0000000000004604

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023873/
https://www.ncbi.nlm.nih.gov/pubmed/27603351
http://dx.doi.org/10.1097/MD.0000000000004604

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