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产前表现为皮尔逊综合征的早产双胞胎。

Preterm twins with antenatal presentation of Pearson syndrome.

作者信息

Castro Leonor, Ferreira Ana C, Cohen Álvaro, Macedo Israel J, Tomé Teresa

机构信息

Pediatric and Neonatal Intensive Care Unit, Hospital Central do Funchal, Av. Luís de Camões, nº 57 - 9004-514 Funchal, Madeira, Portugal.

Metabolic Diseases Unit, Hospital Dona Estefânia, Centro Hospitalar Universitário de Lisboa Central, Lisboa, Portugal.

出版信息

Case Rep Perinat Med. 2022 Feb 1;11(1):20210083. doi: 10.1515/crpm-2021-0083. eCollection 2022 Jan.

Abstract

OBJECTIVES

Pearson syndrome is a mitochondrial cytopathy with multisystemic involvement that typically presents in infancy and has poor prognosis. We aim to present a case that is distinct due to the timing of presentation and associated anomalies.

CASE PRESENTATION

We report the case of preterm monochorionic twins with transfusion dependent fetal anemia that had post-natal multisystem dysfunction which led to the diagnosis of Pearson syndrome.

CONCLUSIONS

This case highlights the possibility of antenatal presentation of Pearson syndrome, which should be considered in cases of severe fetal anemia without an apparent cause.

摘要

目的

皮尔逊综合征是一种累及多系统的线粒体细胞病,通常在婴儿期发病,预后较差。我们旨在报告一例因发病时间和相关异常而具有独特性的病例。

病例报告

我们报告了一对早产单绒毛膜双胎的病例,他们患有输血依赖型胎儿贫血,出生后出现多系统功能障碍,最终诊断为皮尔逊综合征。

结论

该病例突出了皮尔逊综合征产前发病的可能性,在病因不明的严重胎儿贫血病例中应予以考虑。

相似文献

1
Preterm twins with antenatal presentation of Pearson syndrome.产前表现为皮尔逊综合征的早产双胞胎。
Case Rep Perinat Med. 2022 Feb 1;11(1):20210083. doi: 10.1515/crpm-2021-0083. eCollection 2022 Jan.

本文引用的文献

3
Screening and management of thyroid dysfunction in preterm infants.早产儿甲状腺功能障碍的筛查与管理。
Ann Pediatr Endocrinol Metab. 2019 Mar;24(1):15-21. doi: 10.6065/apem.2019.24.1.15. Epub 2019 Mar 31.
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Pearson syndrome.皮尔逊综合征。
Expert Rev Hematol. 2018 Mar;11(3):239-246. doi: 10.1080/17474086.2018.1426454. Epub 2018 Jan 23.
7
Biochemical abnormalities in Pearson syndrome.皮尔逊综合征中的生化异常。
Am J Med Genet A. 2015 Mar;167A(3):621-8. doi: 10.1002/ajmg.a.36939.

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