Magdalena Badura-Stronka, Adam Sebastian Hirschfeld, Evgenia Globa, Anna Winczewska-Wiktor, Anna Potulska-Chromik, Anna Kostera-Pruszczyk, Dorota Wicher, Maciej Robert Krawczyński
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引用次数: 0
摘要
我们报告了三名患有 TBCE 基因 c.100 + 1G > A 变异的患者,并详细描述了他们的临床表型。我们还系统地回顾了所有已知致病性 TBCE 变体患者临床表现的异同文献。在致病性 TBCE 变体患者中观察到的临床表型比以前描述的更为广泛。c.100 + 1G > A 变体的同卵携带者表现出明显较轻的临床病程,在核磁共振成像研究中,钙磷代谢和中枢神经系统病变均无偏差。此外,两名患者表现出高度特异性症状,如脊柱僵硬、嗜酸性粒细胞增多、中性粒细胞减少和夜间低氧血症。此外,男性患者还出现了隐睾症。迄今为止,致病性 c.100 + 1G > A 变异的发现仅限于中东欧后裔患者,这表明该人群中存在潜在的奠基突变。
We report three patients with the novel variant c.100 + 1G > A of the TBCE gene and describe the presented clinical phenotype in detail. We also systematically reviewed the literature for clinical similarities and dissimilarities among all known patients with pathogenic TBCE variants. The clinical phenotype observed in patients with pathogenic TBCE variants is broader than previously described. Homozygous carriers of the c.100 + 1G > A variant exhibit a markedly milder clinical course, with no deviations in the calcium-phosphate metabolism and central nervous system pathology in MRI studies. Additionally, two patients manifest highly specific symptoms such as a rigid spine, eosinophilia, neutropenia, and nocturnal hypoxemia. Furthermore, cryptorchidism was observed in male patients. The identification of the pathogenic c.100 + 1G > A variant has thus far been limited to patients of Central-Eastern European descent, suggesting a potential founder mutation in this population.
期刊介绍:
The Journal of Applied Genetics is an international journal on genetics and genomics. It publishes peer-reviewed original papers, short communications (including case reports) and review articles focused on the research of applicative aspects of plant, human, animal and microbial genetics and genomics.