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三名患有CBL突变患者出现的水肿、胎儿胸腔积液和乳糜胸。

Hydrops, fetal pleural effusions and chylothorax in three patients with CBL mutations.

作者信息

Bülow Luzie, Lissewski Christina, Bressel Rainer, Rauch Anita, Stark Zornitza, Zenker Martin, Bartsch Oliver

机构信息

Institute of Human Genetics, University Medical Centre of the Johannes Gutenberg University, Mainz, Germany.

出版信息

Am J Med Genet A. 2015 Feb;167A(2):394-9. doi: 10.1002/ajmg.a.36838. Epub 2014 Oct 30.

Abstract

Fetal hydrops, fetal pleural effusions, hydrothorax, and chylothorax, may be associated with various genetic disorders, in particular with the Noonan, cardio-facio-cutaneous and Costello syndromes. These syndromes, collectively called RASopathies, are caused by mutations in the RAS/MAPK pathway, which is known to play a major role in lymphangiogenesis. Recently, germline mutations in the Casitas B-cell lymphoma (CBL) gene were reported in 25 patients and of these, 20 had juvenile myelomonocytic leukemia (JMML). The disorder was named "CBL syndrome" or "Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia" (NSLL). To date, prenatal abnormalities have not been reported and it is still debated whether the CBL syndrome falls into the category of a RASopathy, or represents a different entity. Here we report on three unrelated patients with CBL mutations manifesting with hydrops fetalis, fetal pleural effusions and/or congenital hydro-/chylothorax. Our findings further connect the CBL syndrome with the RASopathies.

摘要

胎儿水肿、胎儿胸腔积液、胸腔积水和乳糜胸可能与多种遗传疾病相关,尤其是努南综合征、心脏-颜面-皮肤综合征和科斯特洛综合征。这些综合征统称为RAS病,由RAS/丝裂原活化蛋白激酶(MAPK)信号通路中的突变引起,已知该信号通路在淋巴管生成中起主要作用。最近,在25例患者中报告了卡萨司B细胞淋巴瘤(CBL)基因的种系突变,其中20例患有青少年骨髓单核细胞白血病(JMML)。这种疾病被命名为“CBL综合征”或“伴有或不伴有青少年骨髓单核细胞白血病的努南综合征样疾病”(NSLL)。迄今为止,尚未报道产前异常情况,CBL综合征是否属于RAS病类别或代表不同的疾病实体仍存在争议。在此,我们报告了3例无关患者,他们携带CBL突变,表现为胎儿水肿、胎儿胸腔积液和/或先天性胸腔积水/乳糜胸。我们的研究结果进一步将CBL综合征与RAS病联系起来。

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