{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,14]],"date-time":"2026-04-14T16:43:04Z","timestamp":1776184984888,"version":"3.50.1"},"reference-count":15,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2021,6,23]],"date-time":"2021-06-23T00:00:00Z","timestamp":1624406400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Pediatr."],"abstract":"<jats:p>SHORT syndrome is a rare autosomal dominant disorder characterized by multiple congenital defects and is historically defined by its acronym: <jats:italic>s<\/jats:italic>hort stature, hyperextensibility of joints and\/or inguinal hernia, ocular depression, Rieger anomaly, and teething delay. Herein, we report a male infant with SHORT syndrome who presented with transient neonatal diabetes mellitus (TNDM) with insulin resistance. The proband was born at 38 weeks of gestation but displayed facial dysmorphic features. Intrauterine growth restriction (IUGR) was detected on a prenatal ultrasonography test. His birth weight was 1.8 kg (&amp;lt;3rd percentile), length 44 cm (&amp;lt;3rd percentile), and head circumference 31 cm (&amp;lt;3rd percentile). The patient's blood glucose level started to increase at 5 days of age (218\u2013263 mg\/dl) and remained high at 20 days of age (205\u2013260 mg\/dl). He was treated with subcutaneous insulin and the blood glucose level gradually stabilized. Blood glucose level was stabilized over time without insulin treatment at 6 weeks of age. Clinical exome sequencing showed a heterozygous pathogenic variant, NM_181523.3:c.1945C&amp;gt;T (p.Arg649Trp) in exon 15 of the phosphoinositide-3-kinase regulatory subunit 1 (<jats:italic>PIK3R1<\/jats:italic>) known as the causative gene for SHORT syndrome. Examination of the patient at 10 months of age revealed no hyperglycemic episode and glycated hemoglobin level was 5.2%. To the best of our knowledge, this is the first case of TNDM in SHORT syndrome due to a pathogenic variant of <jats:italic>PIK3R1<\/jats:italic>. We believe that our case can aid in expanding the phenotypes of SHORT syndrome.<\/jats:p>","DOI":"10.3389\/fped.2021.650920","type":"journal-article","created":{"date-parts":[[2021,6,23]],"date-time":"2021-06-23T06:50:36Z","timestamp":1624431036000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":7,"title":["Transient Neonatal Diabetes Mellitus in SHORT Syndrome: A Case Report"],"prefix":"10.3389","volume":"9","author":[{"given":"Shin-Hee","family":"Kim","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Minsung","family":"Kim","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jisook","family":"Yim","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Myungshin","family":"Kim","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dae-Hyun","family":"Jang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1965","published-online":{"date-parts":[[2021,6,23]]},"reference":[{"key":"B1","first-page":"39","article-title":"Malformation syndromes. 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