Congenital fibrous fusion of the jaws (synechiae) with cleft palate: A case report.

Q2 Medicine
W. Alhussin, S. Susnerwala
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引用次数: 0

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.
先天性纤维性颌骨融合(synechiae)伴腭裂:病例报告。
背景先天性上颌下颌融合是一种罕见的疾病。上颌下颌融合通常在新生儿出生后立即被发现,因为新生儿无法正常张口或进食。融合缺损的严重程度不一,从粘膜带(synechiae)到完全骨性融合(syngnathia)不等。病例描述我们报告了一例出生 3 天的男性新生儿先天性齿槽synechiae 合并后腭裂的病例。结论牙龈融合是一种非常罕见的先天性畸形。早期分离纤维带不仅能有效喂养,还能防止面部畸形的发生。然而,这种手术的麻醉可能具有挑战性。
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来源期刊
Journal of neonatal-perinatal medicine
Journal of neonatal-perinatal medicine Medicine-Pediatrics, Perinatology and Child Health
CiteScore
2.00
自引率
0.00%
发文量
124
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