{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,5,13]],"date-time":"2025-05-13T15:22:04Z","timestamp":1747149724387,"version":"3.40.5"},"reference-count":30,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2022,7,10]],"date-time":"2022-07-10T00:00:00Z","timestamp":1657411200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["JIMD Reports"],"published-print":{"date-parts":[[2022,9]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an autosomal recessive mitochondrial disorder characterized by cumulative and progressive gastrointestinal and neurological findings. This retrospective observational study, aimed to explore the time of presentation, diagnosis and clinical follow\u2010up of 13 patients with a confirmed MNGIE disease of Mediterranean origin. The mean age of symptom onset was 7\u2009years (6\u00a0months\u221221\u2009years) and the average diagnosis age was 15.4\u2009years \u00b18.4. Four of 13 patients (30%) died before 30\u2009years at the mean age of 19.7\u2009years \u00b16.8. Cachexia and gastrointestinal symptoms were observed in all patients (100%). The mean body mass index standard deviation score at diagnosis was 4.8\u2009\u00b1\u20092.8. At least three subocclusive episodes were presented in patients who died in last year of their life. The main neurological symptom found in most patients was peripheral neuropathy (92%). Ten patients (77%) had leukoencephalopathy and the remaining three patients without were under 10\u2009years of age. The new homozygous \u201cMediterranean\u201d <jats:italic>TYMP<\/jats:italic> mutation, p.P131L (c.392 C\u2009&gt;\u2009T) was associated with an early presentation and poor prognosis in nine patients (69%) from five separates families. Based on the observations from this Mediterranean MNGIE cohort, we propose that the unexplained abdominal pain combined with cachexia is an indicator of MNGIE. High\u2010platelet counts and nerve conduction studies may be supportive laboratory findings and the frequent subocclusive episodes could be a negative prognostic factor for mortality. Finally, the homozygous p.P131L (c.392 C\u2009&gt;\u2009T) mutation could be associated with rapid progressive disease with poor prognosis.<\/jats:p>","DOI":"10.1002\/jmd2.12315","type":"journal-article","created":{"date-parts":[[2022,7,11]],"date-time":"2022-07-11T05:28:26Z","timestamp":1657517306000},"page":"484-493","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Clinical spectrum of early onset \u201cMediterranean\u201d (homozygous p.<scp>P131L<\/scp> mutation) mitochondrial neurogastrointestinal encephalomyopathy"],"prefix":"10.1002","volume":"63","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9574-7841","authenticated-orcid":false,"given":"Sema","family":"Kalkan U\u00e7ar","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Division of Metabolism and Nutrition Ege University Medical Faculty  Izmir 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