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塞尔努诺斯/XLF 缺陷:一种综合征性原发性免疫缺陷。

Cernunnos/XLF Deficiency: A Syndromic Primary Immunodeficiency.

作者信息

Cipe Funda Erol, Aydogmus Cigdem, Babayigit Hocaoglu Arzu, Kilic Merve, Kaya Gul Demet, Yilmaz Gulec Elif

机构信息

Department of Pediatric Allergy-Immunology, Kanuni Sultan Suleyman Research and Training Hospital, 34303 Istanbul, Turkey.

Department of Genetics, Kanuni Sultan Suleyman Research and Training Hospital, 34303 Istanbul, Turkey.

出版信息

Case Rep Pediatr. 2014;2014:614238. doi: 10.1155/2014/614238. Epub 2014 Jan 8.

Abstract

Artemis, DNA ligase IV, DNA protein kinase catalytic subunit, and Cernunnos/XLF genes in nonhomologous end joining pathways of DNA repair mechanisms have been identified as responsible for radiosensitive SCID. Here, we present a 3-year-old girl patient with severe growth retardation, bird-like face, recurrent perianal abscess, pancytopenia, and polydactyly. Firstly, she was thought as Fanconi anemia and spontaneous DNA breaks were seen on chromosomal analysis. After that DEB test was found to be normal and Fanconi anemia was excluded. Because of that she had low IgG and IgA levels, normal IgM level, and absence of B cells in peripheral blood; she was considered as primary immunodeficiency, Nijmegen breakage syndrome. A mutation in NBS1 gene was not found; then Cernunnos/XLF deficiency was investigated due to clinical similarities with previously reported cases. Homozygous mutation in Cernunnos/XLF gene (NHEJ1) was identified. She is now on regular IVIG prophylaxis and has no new infection. Fully matched donor screening is in progress for bone marrow transplantation which is curative treatment of the disease. In conclusion, the patients with microcephaly, bird-like face, and severe growth retardation should be evaluated for hypogammaglobulinemia and primary immunodeficiency diseases.

摘要

DNA修复机制的非同源末端连接途径中的Artemis、DNA连接酶IV、DNA蛋白激酶催化亚基和Cernunnos/XLF基因已被确定为放射性敏感型重症联合免疫缺陷(SCID)的病因。在此,我们报告一名3岁女童患者,她有严重生长发育迟缓、鸟样面容、复发性肛周脓肿、全血细胞减少和多指畸形。起初,她被认为患有范可尼贫血,染色体分析发现有自发DNA断裂。之后发现双环氧丁烷(DEB)试验正常,排除了范可尼贫血。由于她外周血中IgG和IgA水平低、IgM水平正常且无B细胞,她被认为患有原发性免疫缺陷,即奈梅亨断裂综合征。未发现NBS1基因有突变;然后由于与先前报道病例有临床相似性,对Cernunnos/XLF缺陷进行了调查。确定了Cernunnos/XLF基因(NHEJ1)存在纯合突变。她目前接受定期静脉注射免疫球蛋白预防治疗,没有新的感染。正在进行完全匹配供体的筛查,以便进行骨髓移植,这是该疾病的治愈性治疗方法。总之,对于小头畸形、鸟样面容和严重生长发育迟缓的患者,应评估其低丙种球蛋白血症和原发性免疫缺陷疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04a1/3910469/9050d43782ca/CRIM.PEDIATRICS2014-614238.001.jpg

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