Multiple intestinal atresia and congenital bilateral perisylvian syndrome in a surviving monochorionic twin with intrauterine death of the co-twin

Mochizuki, Kiyofumi; Sato, Masato; Ohhama, Youkatsu; Take, Hiroshi; Kitagawa, Norihiko; Honda, Shohei; Hirata, Yoshihiro; Ishikawa, Hiroshi

doi:10.1016/j.jpedsurg.2010.05.022

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Pathogenesis Of Fetal Structural Defects In Twins1

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“…Although the subjects ultimately had fatal outcomes, data suggest that the immune defect may not be primary, but secondary to intestinal dysfunction. Another report [8] presents a case of a surviving mono-chorionic twin with multiple intestinal atresia and congenital bilateral perisylvian syndrome, which developed after the intrauterine death of the co-twin. The pathology of the placenta demonstrated vein-to-vein communication between the twins and multiple intravascular thrombi in the dead co-twin.…”

Section: Discussionmentioning

confidence: 99%

Enteral Agenesis in an Adult; A Case Presentation

2015

Med. Con.

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Section: Discussionmentioning

confidence: 99%

Enteral Agenesis in an Adult; A Case Presentation

2015

Med. Con.

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“…Some of the most important data supporting vascular mechanisms are summarized below with a focus on the brain. (Hall et al, 2014;Mochizuki et al, 2010;Shue et al, 2012;Stevens & Dobyns, 2004;Yamanouchi et al, 2002).…”

Section: Pathogenesis Of Fetal Structural Defects In Twinsmentioning

confidence: 99%

The spectrum of brain malformations and disruptions in twins

Park

Chapman

Aldinger³

et al. 2020

American J of Med Genetics Pt A

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Twins have an increased risk for congenital malformations and disruptions, including defects in brain morphogenesis. We analyzed data on brain imaging, zygosity, sex, and fetal demise in 56 proband twins and 7 less affected co-twins with abnormal brain imaging and compared them to population-based data and to a literature series. We separated our series into malformations of cortical development (MCD, N = 39), cerebellar malformations without MCD (N = 13), and brain disruptions (N = 11). The MCD group included 37/39 (95%) with polymicrogyria (PMG), 8/39 (21%) with pia-ependymal clefts (schizencephaly), and 15/39 (38%) with periventricular nodular heterotopia (PNH) including 2 with PNH but not PMG. Cerebellar malformations were found in 19 individuals including 13 with a cerebellar malformation only and another 6 with cerebellar

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