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Article type: Case Report
Authors: Alhussin, W.a; * | Susnerwala, S.b
Affiliations: [a] Department of Pediatrics, MD, CABP, Neonatal-Perinatal Fellowship, Division of Neonatology, Zulekha Hospital Sharjah, Sharjah, United Arab Emirates | [b] Department of Neonatology, Sukena Susnerwala, MD, DM, Latifa Women’s and Children’s Hospital, Dubai, United Arab Emirates
Correspondence: [*] Address for correspondence: Walid Alhussin, Department of Pediatrics, MD, CABP, Neonatal-Perinatal Fellowship, Division of Neonatology, Zulekha Hospital Sharjah, United Arab Emirates. Tel.: +971 543882548; Email: [email protected].
Abstract: BACKGROUND:Congenital maxillomandibular fusion is a rare disorder. Maxillomandibular fusion is usually discovered immediately after birth because the newborn is unable to open mouth or feed normally. The fusion defects can present with a wide range of severity, ranging from mucosal band (synechiae) to complete bony fusion (syngnathia). CASE DESCRIPTION:We report a case of congenital alveolar synechiae with posterior cleft palate in a 3-day-old male neonate. The newborn was managed with the help of a multi-disciplinary approach. CONCLUSION:Fusion of the gums is a very rare congenital anomaly. Early division of fibrous bands not only allows effective feeding but also prevents the development of facial deformities. However, anesthesia for this procedure can be challenging.
Keywords: Congenital, cleft palate, fibrous fusion, syngnathia, synechiae
DOI: 10.3233/NPM-230184
Journal: Journal of Neonatal-Perinatal Medicine, vol. 17, no. 4, pp. 607-610, 2024
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