Stricker Sarah, Balmer Cécile, Guzman Raphael, Soleman Jehuda
Department of Neurosurgery, Division of Pediatric Neurosurgery, University Hospital and Children's Hospital of Basel, Spitalstrasse 21, 4031, Basel, Switzerland.
Department of Pediatric Surgery, University Children's Hospital of Basel, Basel, Switzerland.
Childs Nerv Syst. 2019 Apr;35(4):725-728. doi: 10.1007/s00381-018-3990-8. Epub 2018 Oct 22.
Myelomeningocele (MMC) is a common subtype of congenital neural tube defects (NTD). Although congenital malformations including NTD are more common in twins, concordance, especially in dizygotic twins, is extremely rare and is found mostly in same-sex twins. The role of genetic and environmental factors in the etiology of MMC is unclear.
Dizygotic twins of opposite sex were born at term to a 35-year-old woman conceived with in vitro fertilization (IVF) using intracytoplasmic sperm injection (ICSI). Prenatal ultrasonography (US) revealed concordant lumbosacral MMC at 18 weeks of gestation as well as ventriculomegaly and Arnold-Chiari malformation type II at 28 weeks. Both twins underwent surgical repair of the MMC within 48 h after birth and required a ventriculoperitoneal shunt in the second week of life.
The case presented raises questions concerning the etiology of MMC, since in twins, it is compelling to attribute the etiology to genetic factors. In the literature, 22 pairs of twins with concordant MMC have been reported, and of the 10 dizygotic twins described, four were of opposite sex. However, in monozygotic twins, most of the cases are non-concordant; therefore, the role of genetics remains unclear. In addition, environmental factors such as nutrition, metabolic folic acid deficiency, and assisted conception with IVF and ICSI might play a role as well.
The appearance of concordant MMC in opposite-sex dizygotic twins, conceived by IVF using ICSI, intrigues questions concerning the etiology of MMC. In such cases, genetic counseling and evaluation should be considered.
脊髓脊膜膨出(MMC)是先天性神经管缺陷(NTD)的常见亚型。尽管包括NTD在内的先天性畸形在双胞胎中更为常见,但一致性,尤其是在异卵双胞胎中,极为罕见,且大多见于同性双胞胎。遗传和环境因素在MMC病因中的作用尚不清楚。
一名35岁女性通过卵胞浆内单精子注射(ICSI)体外受精(IVF)足月产下一对异性异卵双胞胎。产前超声检查(US)显示,妊娠18周时出现一致的腰骶部MMC,妊娠28周时出现脑室扩大和Ⅱ型阿诺德-奇亚里畸形。双胞胎均在出生后48小时内接受了MMC手术修复,并在出生后第二周需要进行脑室腹腔分流术。
该病例引发了关于MMC病因的问题,因为在双胞胎中,将病因归因于遗传因素很有说服力。文献中报道了22对MMC一致的双胞胎,在描述的10对异卵双胞胎中,有4对是异性。然而,在同卵双胞胎中,大多数病例并不一致;因此,遗传因素的作用仍不清楚。此外,营养、代谢性叶酸缺乏以及IVF和ICSI辅助受孕等环境因素也可能起作用。
通过ICSI进行IVF受孕的异性异卵双胞胎中出现一致的MMC,引发了关于MMC病因的问题。在这种情况下,应考虑进行遗传咨询和评估。