Fetal Tetra-Amelia Birth: A Case Report.

IF 0.6 Q4 OBSTETRICS & GYNECOLOGY
Case Reports in Obstetrics and Gynecology Pub Date : 2024-12-31 eCollection Date: 2024-01-01 DOI:10.1155/crog/7801322
Eyob Asefa Belay, Anberbir Girma Asebot, Bezza Kedida Dabi
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引用次数: 0

Abstract

Fetal limb anomaly presentation varies greatly. It can present as amelia (complete absence of skeletal part of one or more limb), meromelia (partial absence of skeletal part of one or more limb), phocomelia (only rudimentary limb formed), and minor limb disorders like polydactyly. The complete absence of the four fetal limbs is extremely rare. Incidence of tetra-amelia is not well known, but it is mentioned to be 1-4 in 100,000 births in different literature. Etiopathogenesis of fetal tetra-amelia remains speculative. Tetra-amelia occurs either as tetra-amelia syndrome (when other organ systems are affected too) or isolated tetra-amelia. Tetra-amelia syndrome is more common than isolated tetra-amelia. It occurs secondary to genetic aberration or is sporadic. Genetic inheritance of tetra-amelia may present as autosomal dominance, autosomal recessive, or X-linked recessive. The protein coded on WTN 3 on chromosome 17q21 is important for fetal limb and other organ system formation. Mutation associated with the WTN 3 gene is a known cause for fetal limb malformation. Maternal diabetes, amniotic band syndrome, TORCH (toxoplasmosis, rubella cytomegalovirus, herpes simplex, and HIV) infection, alcohol consumption, and intrauterine exposure to some drugs like thalidomide, glucocorticoids, and sedatives are risk factors for limb malformation. Tetra-amelia can be diagnosed as early as the first trimester of pregnancy. Ultrasound imaging is a gold standard investigation to detect tetra-amelia. Tetra-amelia syndrome is associated with high mortality and morbidity than isolated tetra-amelia. In this case report, we present an extremely rare case, isolated tetra-amelia, born to G3P2 (Gravida 3, Para 2) mother at 36 weeks of gestation. It was diagnosed late in pregnancy at 34 weeks. The fetal organs (kidney, lung, abdominal wall, heart, vertebrae, and brain) were evaluated with ultrasound and were found healthy. She gave birth by cesarean section at 36 weeks of gestation for other obstetric indication. Isolated tetra-amelia is an extremely rare case. Early antenatal ultrasound fetal evaluation should be promoted. Early detection of tetra-amelia helps to provide parental counselling and option of management timely. Parental counselling should involve how to care for the neonate with tetra-amelia. Community awareness creation is important to decrease social stigma against babies with tetra-amelia. In such rare cases, it is important to alert public health researchers for possible further epidemiological study.

胎儿四amelia出生:1例报告。
胎儿肢体异常表现差异很大。它可以表现为无肢症(一个或多个肢体的骨骼部分完全缺失)、缺肢症(一个或多个肢体的骨骼部分部分缺失)、缺肢症(仅形成初级肢体)和轻微的肢体疾病,如多指畸形。胎儿四肢完全缺失是极其罕见的。四amelia的发病率并不为人所知,但在不同的文献中提到,每10万名新生儿中有1-4名。胎儿四amelia的发病机制尚不明确。四amelia可以作为四amelia综合征(当其他器官系统也受到影响时)或孤立的四amelia发生。四amelia综合征比孤立的四amelia更常见。继发于遗传畸变或偶发。四amelia的遗传可能表现为常染色体显性、常染色体隐性或x连锁隐性。编码于染色体17q21上的WTN 3蛋白对胎儿肢体和其他器官系统的形成很重要。与WTN 3基因相关的突变是胎儿肢体畸形的已知原因。产妇糖尿病、羊膜带综合征、TORCH(弓形虫病、风疹巨细胞病毒、单纯疱疹和HIV)感染、饮酒以及宫内接触沙利度胺、糖皮质激素和镇静剂等药物是肢体畸形的危险因素。早在怀孕的前三个月就可以诊断出四amelia。超声成像是检测四amelia的金标准。四阿米莉亚综合征的死亡率和发病率高于孤立性四阿米莉亚综合征。在这个病例报告中,我们提出了一个极其罕见的病例,孤立的四amelia,出生在G3P2(妊娠3,Para 2)母亲在妊娠36周。它是在怀孕34周时被诊断出来的。胎儿器官(肾、肺、腹壁、心、椎和脑)经超声检查均健康。由于其他产科指征,她在妊娠36周时剖宫产。孤立的四amelia是一种极其罕见的病例。应提倡早期产前超声胎儿评价。早期发现四amelia有助于及时提供家长咨询和选择管理。父母咨询应包括如何照顾四amelia新生儿。提高社区意识对于减少社会对四amelia婴儿的耻辱感非常重要。在这种罕见的情况下,重要的是要提醒公共卫生研究人员进行进一步的流行病学研究。
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来源期刊
Case Reports in Obstetrics and Gynecology
Case Reports in Obstetrics and Gynecology Medicine-Obstetrics and Gynecology
CiteScore
1.30
自引率
0.00%
发文量
64
审稿时长
12 weeks
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