{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,7]],"date-time":"2026-05-07T12:11:31Z","timestamp":1778155891628,"version":"3.51.4"},"reference-count":7,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2026,1,18]],"date-time":"2026-01-18T00:00:00Z","timestamp":1768694400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"},{"start":{"date-parts":[[2026,1,18]],"date-time":"2026-01-18T00:00:00Z","timestamp":1768694400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["JPGN rep."],"published-print":{"date-parts":[[2026,5]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Menetrier's disease (MD) is a rare, typically transient, hypertrophic gastropathy with under 1000 adult cases and 50 pediatric cases known worldwide. Pediatric cases most often present with an infectious etiology. We present a case of a teenage male expressing a chronic state of disease without infectious origin. Menetrier's most typically causes protein loss and peripheral edema, however, this patient's only expression of disease is an enduring iron deficiency anemia. Moreover, seven additional paternal family members share the same diagnosis. This unique presentation and familial pattern of a very uncommon disease suggests a previously undescribed heritable form of MD. By recording such cases in the medical literature, we aim to boost providers ability to recognize this disease in all its known prior presentations.<\/jats:p>","DOI":"10.1002\/jpr3.70142","type":"journal-article","created":{"date-parts":[[2026,1,19]],"date-time":"2026-01-19T06:05:22Z","timestamp":1768802722000},"page":"259-261","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Menetrier's: A pediatric chronic state of disease with a possible heritable form"],"prefix":"10.1002","volume":"7","author":[{"ORCID":"https:\/\/orcid.org\/0009-0005-9523-9245","authenticated-orcid":false,"given":"MariaElena","family":"Terzis","sequence":"first","affiliation":[{"name":"Department of Pediatrics MaineHealth Portland Maine USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anna","family":"Furr","sequence":"additional","affiliation":[{"name":"Division of Pediatric Gastroenterology MaineHealth Medical Group Portland Maine USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Julia","family":"Fritz","sequence":"additional","affiliation":[{"name":"Division of Pediatric Gastroenterology MaineHealth Medical Group Portland Maine USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2026,1,18]]},"reference":[{"key":"e_1_2_7_2_1","doi-asserted-by":"publisher","DOI":"10.3748\/wjg.v18.i21.2727"},{"issue":"9","key":"e_1_2_7_3_1","article-title":"Clinical and radiological features of Menetrier's disease: a case report and review of the literature","volume":"15","author":"Keener M","year":"2023","journal-title":"Cureus"},{"key":"e_1_2_7_4_1","volume-title":"Menetrier Disease","author":"Gore M","year":"2024"},{"key":"e_1_2_7_5_1","doi-asserted-by":"publisher","DOI":"10.5223\/pghn.2021.24.1.109"},{"key":"e_1_2_7_6_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.cgh.2020.03.017"},{"issue":"10","key":"e_1_2_7_7_1","article-title":"M\u00e9n\u00e9trier's disease and its atypical presentation in four siblings","volume":"14","author":"Hassan IH","year":"2022","journal-title":"Cureus"},{"issue":"10","key":"e_1_2_7_8_1","article-title":"Retraction: M\u00e9n\u00e9trier's disease and its atypical presentation in four siblings","volume":"14","author":"Hassan IH","year":"2023","journal-title":"Cureus"}],"container-title":["JPGN Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/jpr3.70142","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/full-xml\/10.1002\/jpr3.70142","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/jpr3.70142","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,5,7]],"date-time":"2026-05-07T11:30:30Z","timestamp":1778153430000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/jpr3.70142"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,1,18]]},"references-count":7,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2026,5]]}},"alternative-id":["10.1002\/jpr3.70142"],"URL":"https:\/\/doi.org\/10.1002\/jpr3.70142","archive":["Portico"],"relation":{},"ISSN":["2691-171X","2691-171X"],"issn-type":[{"value":"2691-171X","type":"print"},{"value":"2691-171X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,1,18]]},"assertion":[{"value":"2025-09-14","order":0,"name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2025-12-31","order":2,"name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}},{"value":"2026-01-18","order":3,"name":"published","label":"Published","group":{"name":"publication_history","label":"Publication History"}}]}}