Cargando…
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...
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: | |
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 |
Ejemplares similares
-
Importance of early detection of juvenile polyposis syndrome: A case report and literature review
por: Shen, Na, et al.
Publicado: (2020) -
Transthyretin-related hereditary amyloidosis with recurrent vomiting and renal insufficiency as the initial presentation: A case report
por: Xu, Jing, et al.
Publicado: (2017) -
Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China
por: Hu, Hua, et al.
Publicado: (2021) -
Association of single-nucleotide polymorphisms of CDH1 with nonsyndromic cleft lip with or without cleft palate in a northern Chinese Han population
por: Song, Hongquan, et al.
Publicado: (2017) -
Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-Analysis
por: Lu, Ya-Jie, et al.
Publicado: (2015)