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A total of 15 patients cared for at a single center, with a median age of 9.9\u2009years (range 0.25\u201324\u2009years) were included. All patients shared the same founder variant in <jats:italic>GCPC<\/jats:italic> c.1039 C\u2009&gt;\u2009T. The phenotype of this cohort demonstrated good metabolic control with median cohort triglyceride level slightly above normal, no need for continuous overnight feeds, and a higher quality of life compared to a previous GSD cohort. The most frequent complications were oral aversion, gross motor delay, and renal hyperfiltration. We discuss our unique care delivery at a single center that cares for Amish patients with inherited disorders.<\/jats:p>","DOI":"10.1002\/jmd2.12310","type":"journal-article","created":{"date-parts":[[2022,6,21]],"date-time":"2022-06-21T07:34:32Z","timestamp":1655796872000},"page":"453-461","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Glycogen storage disease type 1a in the Ohio Amish"],"prefix":"10.1002","volume":"63","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2129-9422","authenticated-orcid":false,"given":"Ethan M.","family":"Scott","sequence":"first","affiliation":[{"name":"New Leaf Center Clinic for Special Children  Ohio USA"},{"name":"Department of Pediatrics Akron Children's Hospital  Akron Ohio USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Olivia K.","family":"Wenger","sequence":"additional","affiliation":[{"name":"New Leaf Center Clinic for Special Children  Ohio 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