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贝克威思-维德曼综合征双胞胎表型谱的诊断与管理

Diagnosis and management of the phenotypic spectrum of twins with Beckwith-Wiedemann syndrome.

作者信息

Cohen Jennifer L, Duffy Kelly A, Sajorda Brian J, Hathaway Evan R, Gonzalez-Gandolfi Christina X, Richards-Yutz Jennifer, Gunter Andrew T, Ganguly Arupa, Kaplan Julie, Deardorff Matthew A, Kalish Jennifer M

机构信息

Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Am J Med Genet A. 2019 Jul;179(7):1139-1147. doi: 10.1002/ajmg.a.61164. Epub 2019 May 8.

Abstract

Beckwith-Wiedemann syndrome (BWS) is an overgrowth disorder with a heterogeneous phenotypic spectrum. There is an increased prevalence of monozygotic twinning in BWS. Given the epigenetic nature and phenotypic spectrum that defines BWS, twins are often discordant for clinical features, and clinicians are faced with the challenge of diagnosing and managing these twins. We present a cohort of multiple pregnancies in which one or more child from each pregnancy was diagnosed with BWS. We conducted a chart review of monochorionic and dichorionic gestations. Clinical scores for monochorionic twins demonstrated phenotypic discordance between the proband and twin. Based on linear regression analysis, a higher clinical score in the proband correlated with larger phenotypic discordance between twin siblings. Despite phenotypic discordance, however, we observed a consistent additive clinical score for a pregnancy (proband's plus twin's scores from a pregnancy). This idea of a finite degree of affectedness for a pregnancy implies a finite number of epigenetically affected cells. This further corroborates the idea that timing of monozygotic monochorionic twinning correlates with the disruption of establishment and/or maintenance of imprinting. The difference in clinical score between a proband and their twin may be due to diffused mosaicism, whereby there is an asymmetric distribution of affected cells among the multiple fetuses in a monozygotic monochorionic pregnancy, leading to a spectrum of variably affected phenotypes. Based on these findings, we recommend an algorithm for a conservative approach to clinically evaluate all children in a monozygotic multiple gestation affected by BWS.

摘要

贝克威思-维德曼综合征(BWS)是一种具有异质表型谱的过度生长障碍。BWS中单卵双胎的发生率增加。鉴于定义BWS的表观遗传性质和表型谱,双胞胎在临床特征上往往不一致,临床医生面临着诊断和管理这些双胞胎的挑战。我们报告了一组多胎妊娠病例,其中每个妊娠中有一个或多个孩子被诊断为BWS。我们对单绒毛膜和双绒毛膜妊娠进行了病历回顾。单绒毛膜双胞胎的临床评分显示先证者与双胞胎之间存在表型不一致。基于线性回归分析,先证者较高的临床评分与双胞胎兄弟姐妹之间较大的表型不一致相关。然而,尽管存在表型不一致,我们观察到一个妊娠(先证者加同一妊娠中双胞胎的评分)的临床评分具有一致的累加性。这种关于妊娠有限程度受影响的观点意味着表观遗传受影响细胞的数量有限。这进一步证实了单卵单绒毛膜双胎的时间与印记建立和/或维持的破坏相关的观点。先证者与其双胞胎之间临床评分的差异可能是由于弥漫性镶嵌现象,即在单卵单绒毛膜妊娠的多个胎儿中,受影响细胞存在不对称分布,导致一系列不同程度受影响的表型。基于这些发现,我们推荐一种算法,采用保守方法对受BWS影响的单卵多胎妊娠中的所有儿童进行临床评估。

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