The etiopathogenic and morphological spectrum of anencephaly: a comprehensive review of literature

被引:15
作者
Munteanu, Octavian [1 ]
Cirstoiu, Monica Mihaela [2 ,3 ]
Filipoiu, Florin Mihail [1 ]
Neamtu, Maria Narcisa [4 ]
Stavarache, Irina [5 ]
Georgescu, Tiberiu Augustin [6 ,7 ]
Bratu, Ovidiu Gabriel [8 ]
Iorgulescu, Gabriela [9 ]
Bohiltea, Roxana Elena [2 ,3 ]
机构
[1] Carol Davila Univ Med & Pharm, Dept Anat, Bucharest, Romania
[2] Carol Davila Univ Med & Pharm, Dept Obstet & Gynecol, Bucharest, Romania
[3] Univ Emergency Hosp, Dept Obstet & Gynecol, Bucharest, Romania
[4] Carol Davila Univ Med & Pharm, Bucharest, Romania
[5] Fundeni Clin Inst, Dept Radiol, Bucharest, Romania
[6] Carol Davila Univ Med & Pharm, Dept Pathol, Bucharest, Romania
[7] Polizu Clin Hosp, Dept Pathol, Bucharest, Romania
[8] Carol Davila Univ Med & Pharm, Dept Urol, Bucharest, Romania
[9] Carol Davila Univ Med & Pharm Bucharest, Dept Behav Sci, Bucharest, Romania
关键词
anencephaly; folic acid; genetic polymorphism; NEURAL-TUBE DEFECTS; 3-DIMENSIONAL ULTRASOUND; GENE POLYMORPHISMS; 1ST TRIMESTER; SPINA-BIFIDA; PREGNANCY; DIAGNOSIS; ANOMALIES; RISK; MALFORMATIONS;
D O I
10.47162/RJME.61.2.03
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Anencephaly is a severe malformation of the central nervous system (CNS), being one of the most common types of neural tube defects. It is defined as total or partial absence of the calvarium, with absence of the brain. Anencephaly has an incidence of 1 to 5 in every 1000 births, and the mortality rate is 100% during intrauterine life or within hours or days after birth. The etiology of anencephaly remains unclear, but various maternal-related environmental and genetic risk factors have been reported, which include diabetes, obesity, exposure to different drugs or toxins, genetic polymorphisms and mutations, as well as positive family history for neural tube defects. One of the most important nutritional factors in the development of anencephaly is folate deficiency. Methylenetetrahydrofolate reductase (MTHFR) gene codes the enzyme involved in the intracellular metabolism of folic acid; the 677C-T polymorphism of this gene causes the thermolability of the enzyme and decreased enzymatic activity, which is also dependent of folate plasmatic level. Etiopathogenesis of anencephaly includes several mutations in various other genes, such as: platelet-derived growth factor receptor alpha (PDGFRA), cadherin epidermal growth factor (EGF) laminin G (LAG) seven-pass G-type receptor 1 (CELSR1), Vang-like 1 (VANGLI) and Vang-like 2 (VANGL2), the last two being involved in the process of neurulation. Screening tests include maternal serum alpha-fetoprotein level and ultrasound (US) examination. During the first trimester US screening, anencephaly is now detected in all cases, but in order to decrease the complication rate of pregnancy termination, the diagnosis should be established as soon as possible, during the pregnancy confirmation US. We conclude that given that anencephaly is a severe malformation of the CNS, morphological characterization could improve the screening by US that is mandatory in the first trimester in order to plan the best, safe and early management.
引用
收藏
页码:335 / 343
页数:9
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