与ASPA基因新突变相关的Canavan病白质筛状外观

IF 0.4 Q4 PEDIATRICS
Journal of pediatric genetics Pub Date : 2021-03-10 eCollection Date: 2022-12-01 DOI:10.1055/s-0041-1725118
Maya Dattatraya Bhat, Netravathi Manjunath, Renu Kumari, Mohammed Faruq, Pramod Kumar Pal, Chandrajit Prasad, Ravindranadh Chowdary Mundlamuri, Atchayaram Nalini, Gautham Arunachal Udupi, Priyanka Priyadarshini Baishya, Karthik Kulanthaivelu
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引用次数: 2

摘要

Canavan病的筛状脑外观是一种罕见的发现。这两个病例拓宽了磁共振成像(MRI)的表型,在半瓣中央、脑室周围和叶状白质中发现了许多椭圆形、囊性结构,一些类似扩张的Virchow-Robin (VR)空间,形成筛网状。此外,在第二例的灰质连接处存在离散的圆形至椭圆形囊肿,其较大且形态上与VR空间不同。这些囊肿在影像学上没有在任何平面上拉长,更能代表巨大的髓内液泡。基因分析揭示了天冬氨酸酰化酶或ASPA基因的新突变,这可能解释了Canavan病的严重形式,这可能解释了成像结果。Canavan病中白质的多囊性表现是不寻常的,可能代表了两种不同的组织病理基质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cribriform Appearance of White Matter in Canavan Disease Associated with Novel Mutations of ASPA Gene.

Cribriform appearance of the brain in Canavan disease is a rare finding. The two presented cases broaden the magnetic resonance imaging (MRI) phenotype wherein numerous oval, cystic structures, a few resembling dilated Virchow-Robin (VR) spaces, were noted in the centrum semiovale, periventricular, and lobar white matter producing a cribriform pattern. Besides, discrete round to oval cysts were present at the gray-white matter junctions in the second case, which were larger and appeared morphologically distinct from the VR spaces. These cysts did not elongate in any plane on imaging and were more representative of giant intramyelinic vacuoles. Genetic analysis revealed novel mutations in the aspartoacylase or ASPA gene that possibly accounts for the severe form of Canavan disease, which probably explains the imaging findings. The multicystic appearance of the white matter in Canavan disease is unusual and possibly represents two different histopathological substrates.

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来源期刊
自引率
0.00%
发文量
32
期刊介绍: The Journal of Pediatric Genetics is an English multidisciplinary peer-reviewed international journal publishing articles on all aspects of genetics in childhood and of the genetics of experimental models. These topics include clinical genetics, molecular genetics, biochemical genetics, medical genetics, dysmorphology, teratology, genetic counselling, genetic engineering, formal genetics, neuropsychiatric genetics, behavioral genetics, community genetics, cytogenetics, hereditary or syndromic cancer genetics, genetic mapping, reproductive genetics, fetal pathology and prenatal diagnosis, multiple congenital anomaly syndromes, and molecular embryology of birth defects. Journal of Pediatric Genetics provides an in-depth update on new subjects and current comprehensive coverage of the latest techniques used in the diagnosis of childhood genetics. Journal of Pediatric Genetics encourages submissions from all authors throughout the world. The following articles will be considered for publication: editorials, original and review articles, short report, rapid communications, case reports, letters to the editor, and book reviews. The aim of the journal is to share and disseminate knowledge between all disciplines in the field of pediatric genetics. This journal is a publication of the World Pediatric Society: http://www.worldpediatricsociety.org/ The Journal of Pediatric Genetics is available in print and online. Articles published ahead of print are available via the eFirst service on the Thieme E-Journals platform.
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