Van Der Woude综合征伴外胚层发育不良1例报告

D. Mg, Manoharan Gvmg, Lakshmi Kb
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引用次数: 0

摘要

先天性下唇凹陷是一种罕见的发育畸形,具有高外显率、可变表达性和常染色体显性。Van der Woude综合征的主要征象是先天性下唇凹陷、唇裂伴或不伴腭裂和孤立性腭裂。下颌缺失是与该综合征相关的主要特征。外胚层发育不良(ED)是一种罕见的遗传性疾病,表现为头发、皮肤、牙齿和汗腺的缺陷。在ED中,原胚外胚层衍生物衍生的组织发育存在缺陷。皮肤干燥和头发稀疏是这些患者的共同特征。据报道,外胚层发育不良患者牙齿部分或完全缺失。这是一个18岁的男性病例报告,合并了Van der Woude综合征(VWS)和少汗性外胚层发育不良(HED)的特征。这个病人在很小的时候就接受了手术治疗唇裂。
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Van Der Woude Syndrome with Ectodermal Dysplasia- Case Report
Congenital lip pits of the lower lip are rare developmental malformation with high penetrance, variable expressivity, and autosomal dominance. The cardinal signs in Van der Woude syndrome are congenital lower lip pits, cleft lip with or without cleft palate, and isolated cleft palate. Hypodontia is a cardinal feature that is associated with this syndrome. Ectodermal Dysplasia (ED) is a rare group of inherited disorders manifested with a defect in hair, skin, teeth, and eccrine glands. In ED there are defects in the development of tissues derived from primary embryonic ectodermal derivatives. Dry skin and sparse hair are common features seen in these patients. Partial or complete absence of teeth is reported in ectodermal dysplasia. This is a case report of an 18-year-old male with combined features of Van der Woude Syndrome (VWS) and Hypohidrotic Ectodermal Dysplasia (HED). The patient was surgically managed for the cleft lip at an early age.
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