一例罕见的胎儿神经管缺陷:后脑畸形

S. Elsirgany, S. Salama, M. Aboulghar
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引用次数: 0

摘要

无脑畸形的特征是由于脊柱畸形导致的严重的头部向后弯曲和颈部缺失,被认为是罕见的异常。患病率:0.1-10:10万,男:女。病因:未知,但涉及遗传、环境因素。发病机理:未知。复发风险:1-4%。相关异常:无脑畸形、脑膨出、独眼畸形、下颌缺骨、腭裂、关节挛缩、畸形足、前脑畸形、脊柱裂、肺发育不全、脐膨出、胃裂、心血管疾病、先天性膈疝、胃肠闭锁、脐动脉单侧、肾脏异常。结论:脑后畸形是一种致死性先天性神经管畸形。其特点是枕骨缺损,胎儿头固定后屈和颈胸椎严重前凸。鉴别诊断:包括无脑畸形伴颈椎后屈和klippel - field综合征
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case of a fetal neural tube defect: Iniencephaly
Iniencephaly is characterized by severe retro flexion of the head with the absence of neck due to spinal vertebrae deformities, it is considered as uncommon anomaly. Prevalence: 0.1-10:10,000, M:F. Etiology: Unknown, but genetic, environmental factors are implicated. Pathogenesis: Unknown. Recurrence risk: 1-4%. Associated anomalies: Anencephaly, encephalocele, cyclopedia, lack of lower jaw bone, cleft palate, arthrogryposis, clubfeet, holoprosencephaly, spina bifida, lung hypoplasia, omphalocele, gastroschisis, cardiovascular disorders, Congenital diaphragmatic hernias, gastrointestinal atresia, single umbilical artery and renal abnormalities. Conclusion: Iniencephaly is a lethal congenital neural tube malformation. It is characterized by occipital bone defect, fixed retroflexion of the fetal head and severe lordosis of the cervicothoracic spine. Differential diagnosis: Include anencephaly with cervical spinal retro flexion and Klippel-Fiel syndrome
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