{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,11]],"date-time":"2025-12-11T03:23:27Z","timestamp":1765423407184,"version":"build-2065373602"},"reference-count":14,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2023,3,11]],"date-time":"2023-03-11T00:00:00Z","timestamp":1678492800000},"content-version":"vor","delay-in-days":69,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Case Reports in Pediatrics"],"published-print":{"date-parts":[[2023,1]]},"abstract":"<jats:p>Microdeletion of the short arm of chromosome 18 is one of the most common chromosome deletion syndromes. Its estimated frequency is 1 in 50,000 live\u2010born infants, with female prevalence over males. Around 150 cases have been described till now. The reported abnormalities include growth deficiency, hypotonia, microcephaly, dysmorphic facial features such as ptosis, epicanthal folds, hypertelorism and micrognathia, and relatively small hands and feet. Our patient was a full\u2010term low birth weight (2150\u2009gm) female newborn, showing cleft upper lip and palate (hard and soft palate), bilateral congenital Talipes Equinovarus with rocker bottom foot, microcephaly, atrial septal defect. She was initially conservatively managed with gavage feeding, then shifted into paladai feeding of expressed breast milk. A multidisciplinary approach was adopted due to various malformations and for the potential occurring complications. To our knowledge, this is the first case diagnosed during the neonatal period.<\/jats:p>","DOI":"10.1155\/2023\/2275582","type":"journal-article","created":{"date-parts":[[2023,3,11]],"date-time":"2023-03-11T15:20:09Z","timestamp":1678548009000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["A Neonatal Patient Diagnosed with Chromosome 18p 11.1 Microdeletion Syndrome Presented with Trisomy 18Like Phenotype"],"prefix":"10.1155","volume":"2023","author":[{"given":"Deepa","family":"Banker","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6219-9671","authenticated-orcid":false,"given":"Bhavdeep","family":"Mungala","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zankhana","family":"Parekh","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shachi","family":"Ganatra","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Vimal","family":"Maheshwari","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yashica","family":"Raj","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Utsav","family":"Patel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Digant","family":"Patel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kishan","family":"Chamar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Vasu","family":"Solanki","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2023,3,11]]},"reference":[{"unstructured":"WHO Birth defects 2022 https:\/\/www.who.int\/news-room\/fact-sheets\/detail\/birth-defects.","key":"e_1_2_7_1_2"},{"volume-title":"Smith\u2019s Recognizable Patterns of Human Malformation","year":"2013","author":"Jones K. L.","key":"e_1_2_7_2_2"},{"unstructured":"BacinoC. A. Microdeletion syndromes (chromosomes 12 to 22) 2022 https:\/\/www.uptodate.com\/contents\/microdeletion-syndromes-chromosomes-12-to-22?search=microdeletion-syndromes-chromosomes-12-to%2022&source=search_result&selectedTitle=1%7E150&usage_type=default&display_rank=1#H1968950.","key":"e_1_2_7_3_2"},{"doi-asserted-by":"publisher","key":"e_1_2_7_4_2","DOI":"10.1186\/1471-2431-13-59"},{"volume-title":"Cleft Lip and Palate: Developmental Abnormalities of the Face, Mouth and Jaws - Bailey and Love\u2019s Short Practice of Surgery","author":"Williams N. S.","key":"e_1_2_7_5_2"},{"doi-asserted-by":"publisher","key":"e_1_2_7_6_2","DOI":"10.4103\/ccd.ccd_129_17"},{"volume-title":"Abnormalities of Chromosome Structure - Nelson Textbook of Pediatrics","year":"2020","author":"Bacino C. 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