磁共振成像在罕见遗传性疾病(即色素失禁症, 也称布洛赫-苏兹伯格综合征)诊断中的应用: 临床病例
- 作者: Yarmola I.I.1, Anikin A.V.1, Gankin D.A.2, Fomina L.E.1, Kharitonova N.A.1, Zhanin I.S.1, Pushkov A.A.1, Basargina M.A.1, Kondakova O.B.1
 - 
							隶属关系: 
							
- National Medical Research Center for Children's Health
 - Shchelkovsky Perinatal Center
 
 - 期: 卷 4, 编号 3 (2023)
 - 页面: 384-392
 - 栏目: 临床病例及临床病例的系列
 - URL: https://bakhtiniada.ru/DD/article/view/254076
 - DOI: https://doi.org/10.17816/DD430154
 - ID: 254076
 
如何引用文章
详细
色素失禁症(布洛克-苏兹伯格综合征,Bloch-Sulzberger Syndrome)是一种罕见的遗传性疾病,表现为特征性皮疹以及其他器官和系统的损坏。磁共振成像是显示出大脑结构病变和预测儿童神经系统表现的优先方法。
皮肤科医生在色素失禁症的诊断中起着关键作用;需要通过对IKBKG基因进行分子遗传分析,以确诊。
一名新生女婴患有典型的布洛赫-苏兹伯格综合征皮疹和IKBKG基因缺失,在进行脑磁共振成像检查后,医生发现了多处缺血、出血和传导通路病变。
布洛赫-苏兹伯格综合征患者的脑磁共振成像可用于评估脑物质损坏的严重程度,这有助于解释神经症状的原因、调整康复措施和预测患儿的发展。
关键词
作者简介
Igor I. Yarmola
National Medical Research Center for Children's Health
							编辑信件的主要联系方式.
							Email: lord_dukich@bk.ru
				                	ORCID iD: 0000-0002-1272-5119
				                	SPIN 代码: 5591-8066
																		                												                	俄罗斯联邦, 							Moscow						
Anatoly V. Anikin
National Medical Research Center for Children's Health
														Email: anikacor@gmail.com
				                	ORCID iD: 0000-0003-0362-6511
				                	SPIN 代码: 7592-1352
																		                								
MD, Cand. Sci. (Med.)
俄罗斯联邦, MoscowDmitry A. Gankin
Shchelkovsky Perinatal Center
														Email: ganja-nn@yandex.ru
				                	ORCID iD: 0009-0001-6779-8702
				                																			                												                	俄罗斯联邦, 							Schelkovo						
Lyubov E. Fomina
National Medical Research Center for Children's Health
														Email: love.fomina@mail.ru
				                	ORCID iD: 0000-0002-3838-3284
				                	SPIN 代码: 1298-8350
																		                												                	俄罗斯联邦, 							Moscow						
Natalia A. Kharitonova
National Medical Research Center for Children's Health
														Email: kharitonovan@nczd.ru
				                	ORCID iD: 0000-0002-6912-1471
				                	SPIN 代码: 7379-8269
																		                								
MD, Cand. Sci. (Med.)
俄罗斯联邦, MoscowIlya S. Zhanin
National Medical Research Center for Children's Health
														Email: zhaninis@nczd.ru
				                	ORCID iD: 0000-0003-1423-0379
				                	SPIN 代码: 6108-2016
																		                								
MD, Cand. Sci. (Med.)
俄罗斯联邦, MoscowAleksandr A. Pushkov
National Medical Research Center for Children's Health
														Email: n1972z@yandex.ru
				                	ORCID iD: 0000-0001-6648-2063
				                	SPIN 代码: 2928-5764
																		                								
Cand. Sci. (Biol.)
俄罗斯联邦, MoscowMilana A. Basargina
National Medical Research Center for Children's Health
														Email: kharitonovan@nczd.ru
				                	ORCID iD: 0000-0003-2075-6668
				                	SPIN 代码: 5504-7154
																		                								
MD, Cand. Sci. (Med.)
俄罗斯联邦, MoscowOlga B. Kondakova
National Medical Research Center for Children's Health
														Email: n1972z@yandex.ru
				                	ORCID iD: 0000-0002-6316-9992
				                	SPIN 代码: 9066-3698
																		                								
MD, Cand. Sci. (Med.)
俄罗斯联邦, Moscow参考
- Scheuerle AE, Ursini MV, Adam MP, et al. Incontinentia Pigmenti. In: GeneReviews [Internet], Seattle (WA): University of Washington, Seattle; 1993.
 - Fusco F. Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-B activation. Hum Mol Genet. 2004;13(16):1763–1773. doi: 10.1093/hmg/ddh192
 - Yadlapati S, Tripathy K. Incontinentia pigmenti (Bloch Sulzberger Syndrome). In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2023.
 - Savostyanov KV. Modern algorithms of genetic diagnosis of rare hereditary diseases in Russian patients. Moscow: Polygraphist Publisher; 2022. 451 р. (In Russ).
 - Minić S, Cerovac N, Novaković I, et al. The impact of the IKBKG gene on the appearance of the corpus callosum abnormalities in incontinentia pigmenti. Diagnostics. 2023;13(7):1300. doi: 10.3390/diagnostics13071300
 - Chistiakov DA, Savostanov KV, Kuzenkova LM, et al. Molecular characteristics of patients with glycosaminoglycan storage disorders in Russia. Clin Chim Acta. 2014;(436):112–120. doi: 10.1016/j.cca.2014.05.010
 - Chistyakov DA, Savostanov KV, Nosikov VV, Turakulov RI. Genetic determinants of Graves’ disease. Mol Gen Metabol. 2000;71(1-2):66–69. doi: 10.1006/mgme.2000.3042
 - Meuwissen ME, Mancini GM. Neurological findings in incontinentia pigmenti: A review. Eur J Med Genet. 2012;55(5):323–331. doi: 10.1016/j.ejmg.2012.04.007
 - Carney RG. Incontinentia pigmenti. A world statistical analysis. Arch Dermatol. 1976;112(4):535–542.
 - Minić S, Trpinac D, Obradović M. Incontinentia pigmenti diagnostic criteria update. Clin Genet. 2014;85(6):536–542. doi: 10.1111/cge.12223
 - Haque MN, Ohtsubo M, Nishina S, et al. Analysis of IKBKG/NEMO gene in five Japanese cases of incontinentia pigmenti with retinopathy: Fine genomic assay of a rare male case with mosaicism. J Hum Genet. 2021;66(2):645–645. doi: 10.1038/s10038-020-00836-3
 - Kawai M, Kato T, Tsutsumi M, et al. Molecular analysis of low-level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia Pigmenti. Mol Genet Genomic Med. 2020;8(12):e1531. doi: 10.1002/mgg3.1531
 - Tak PP, Firestein GS. NF-κB: A key role in inflammatory diseases. J Clin Invest. 2001;107(1):7–11. doi: 10.1172/JCI11830
 - Kleinman JT. Early Wallerian degeneration on magnetic resonance imaging: Underappreciated but highly relevant. Dev Med Child Neurol. 2013;55(2):104–105. doi: 10.1111/dmcn.12022
 - Salamon SA, Lichtenbelt K, Cowan FM, et al. Clinical presentation and spectrum of neuroimaging findings in newborn infants with incontinentia pigmenti. Dev Med Child Neurol. 2016;58(10):1076–1084. doi: 10.1111/dmcn.13140
 - Lou H, Zhang L, Xiao W, et al. Nearly completely reversible brain abnormalities in a patient with incontinentia pigmenti. Am J Neuroradiol. 2008;29(3):431–433. doi: 10.3174/ajnr.A0890
 - Kinoshita T, Ogawa T, Yoshida Y, et al, Curvilinear T1 hyperintense lesions representing cortical necrosis after cerebral infarction. Neuroradiology. 2005;47(7):647–651. doi: 10.1007/s00234-005-1398-0
 - Hauw JJ, Perié G, Bonnette J, Escourolle R. [Neuropathological study of incontinentia pigmenti. Anatomical case report (author’s transl). (In French)]. Acta Neuropathol. 1977;38(2):159–162. doi: 10.1007/BF00688564
 
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