孤立性大口畸形伴双侧面裂一例早产儿

IF 0.2 Q4 PEDIATRICS Journal of Clinical Neonatology Pub Date : 2023-07-01 DOI:10.4103/jcn.jcn_30_23
Prashanth Raghavendra, Sruthi S. Nair, A. Haribalakrishna, Revati Tekwani
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引用次数: 0

摘要

面部裂隙是一种罕见的表现,与软组织和骨骼异常相关的口腔面部区域缺陷。这种情况有多种表现,通常会导致美观问题和喂养困难,影响生长和营养。我们描述了一例早产新生儿,诊断为非综合征性Tessier 7型孤立性双侧面裂。评估显示,巨大畸形伴有软组织和皮肤受累,肌肉组织、上颌骨、下颌骨和其他面部骨骼正常。及时识别和评估这一早产新生儿有助于更好地管理这种情况。长期随访仍然至关重要,因为整形手术指导下的美容康复、喂养和言语治疗评估是提高生活质量的必要条件。
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Isolated macrostomia with bilateral facial cleft in a preterm neonate
Facial clefts are a rare presentation with defects of the orofacial region associated with abnormalities in the soft tissues and bones. This condition has a variable presentation, often leading to aesthetic problems and feeding difficulty that affect growth and nutrition. We describe a preterm neonate diagnosed with nonsyndromic Tessier type 7 isolated bilateral facial clefts. The evaluation revealed a macrostomia with soft tissue and skin involvement with normal musculature, maxillae, mandible, and other facial bones. Timely recognition and evaluation of this premature neonate aided in better management of this condition. Long-term follow-up remains essential as plastic surgery-guided cosmetic rehabilitation, feeding, and speech therapy assessment are required for a better quality of life.
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期刊介绍: The JCN publishes original articles, clinical reviews and research reports which encompass both basic science and clinical research including randomized trials, observational studies and epidemiology.
期刊最新文献
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