{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,12]],"date-time":"2026-10-12T13:46:06Z","timestamp":1791812766553,"version":"4.3.4"},"reference-count":5,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"Suppl 3","license":[{"start":{"date-parts":[[2026,9,15]],"date-time":"2026-09-15T00:00:00Z","timestamp":1789430400000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2026,10]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    Hereditary pancreatitis is a rare genetic disorder, usually associated with gain-of-function mutations in the PRSS1 gene. While in the Indian pediatric population, the SPINK1 mutations are more frequently reported, making PRSS1 mutations, particularly the\n                    <jats:italic toggle=\"yes\">de novo<\/jats:italic>\n                    variants, rare. An 11-year-old school-going Indian girl presented with recurrent acute pancreatitis beginning at the age of 5 years. This progressed to chronic pancreatitis by the age of 10 years. Metabolic, autoimmune, structural, and infectious causes were excluded. The genetic test done revealed a heterozygous pathogenic PRSS1 c.86A&gt;T (p.Asn29Ile) variant. In the absence of family history, this was consistent with a likely\n                    <jats:italic toggle=\"yes\">de novo<\/jats:italic>\n                    mutation. No pathogenic variants were detected in\n                    <jats:italic toggle=\"yes\">SPINK1<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">CFTR<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">CTRC<\/jats:italic>\n                    , or\n                    <jats:italic toggle=\"yes\">CPA1<\/jats:italic>\n                    . Pancreatic enzyme replacement therapy and dietary modification reduced the frequency of attacks and preserved her growth. This case highlights the importance of genetic evaluation in children who present with unexplained recurrent pancreatitis, even when there is no positive family history. Early identification of PRSS1 mutation allows for appropriate counseling, long-term surveillance, and complication prevention.\n                  <\/jats:p>","DOI":"10.4103\/aam.aam_191_26","type":"journal-article","created":{"date-parts":[[2026,9,16]],"date-time":"2026-09-16T04:00:19Z","timestamp":1789531219000},"page":"S468-S470","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["De novo PRSS1 p.Asn29Ile Mutation Causing Hereditary Pancreatitis in an Indian Child"],"prefix":"10.4103","volume":"25","author":[{"given":"Vineeta","family":"Pande","sequence":"first","affiliation":[{"name":"Department of Paediatrics, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Pune, Maharashtra, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nidhi N.","family":"Upadhyaya","sequence":"additional","affiliation":[{"name":"Department of Paediatrics, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Pune, Maharashtra, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bharath Sinha","family":"Reddy","sequence":"additional","affiliation":[{"name":"Department of Paediatrics, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Pune, Maharashtra, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amrita","family":"Nepram","sequence":"additional","affiliation":[{"name":"Department of Paediatrics, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Pune, Maharashtra, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2026,9,15]]},"reference":[{"key":"R1-20261012","doi-asserted-by":"crossref","first-page":"286","DOI":"10.1006\/bbrc.2000.3797","article-title":"Gain-of-function mutations associated with hereditary pancreatitis enhance autoactivation of human cationic trypsinogen","volume":"278","author":"Sahin-T\u00f3th","year":"2000","journal-title":"Biochem Biophys Res Commun"},{"key":"R2-20261012","doi-asserted-by":"crossref","first-page":"11788","DOI":"10.3748\/wjg.v20.i33.11788","article-title":"PRSS1 and SPINK1 mutations in idiopathic chronic and recurrent acute pancreatitis","volume":"20","author":"Pelaez-Luna","year":"2014","journal-title":"World J Gastroenterol"},{"key":"R3-20261012","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1097\/MPG.0000000000002661","article-title":"The INSPPIRE cohort: Pediatric acute recurrent pancreatitis and chronic pancreatitis across regions","volume":"71","author":"Dike","year":"2020","journal-title":"J Pediatr Gastroenterol Nutr"},{"key":"R5-20261012","first-page":"524","article-title":"The management of acute pancreatitis in the pediatric population: A clinical report from NASPGHAN Pancreas Committee","volume":"18","author":"Abu-El-Haija","year":"2018","journal-title":"Pancreatology"},{"key":"R6-20261012","doi-asserted-by":"crossref","first-page":"1","DOI":"10.5409\/wjcp.v11.i1.27","article-title":"Hereditary pancreatitis: An updated review in pediatrics","volume":"11","author":"Panchoo","year":"2022","journal-title":"World J Clin Pediatr"}],"container-title":["Annals of African Medicine"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.4103\/aam.aam_191_26","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,10,12]],"date-time":"2026-10-12T13:01:15Z","timestamp":1791810075000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/aam.aam_191_26"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,9,15]]},"references-count":5,"journal-issue":{"issue":"Suppl 3","published-print":{"date-parts":[[2026]]}},"URL":"https:\/\/doi.org\/10.4103\/aam.aam_191_26","relation":{},"ISSN":["1596-3519","0975-5764"],"issn-type":[{"value":"1596-3519","type":"print"},{"value":"0975-5764","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,9,15]]},"assertion":[{"value":"2026-02-22","name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2026-03-23","name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}}]}}