Hélène Morel, Laurent Bailly, Cédric Urbanczyk, Dominique Hervé, Stéphane Berroir, Raphaël Le Bouc, Richard Levy, Mylène Meyer, Chaker Aloui, Elisabeth Tournier-Lasserve, Guillaume Mathey
{"title":"新描述的末端截断LAMB1变异的临床放射谱的扩展。","authors":"Hélène Morel, Laurent Bailly, Cédric Urbanczyk, Dominique Hervé, Stéphane Berroir, Raphaël Le Bouc, Richard Levy, Mylène Meyer, Chaker Aloui, Elisabeth Tournier-Lasserve, Guillaume Mathey","doi":"10.1212/NXG.0000000000200069","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>To refine the clinical spectrum of a very recently identified phenotype associated with <i>LAMB1</i> end-truncating pathogenic variations.</p><p><strong>Methods: </strong>Detailed clinical, neuropsychological, and MRI investigation of 6 patients from 2 unrelated families segregating end-truncating <i>LAMB1</i> variations.</p><p><strong>Results: </strong>All patients harbored <i>a LAMB1</i> end-truncating pathogenic variation. The specific association of a hippocampal type episodic memory dysfunction and a diffuse leukoencephalopathy was observed in all 4 patients aged older than 50 years, slightly worsening over time in 2 patients with several years of follow-up. Additional unspecific neurologic symptoms are reported, such as episodes of numbness, language troubles, or faintness in these 4 patients and the 2 younger ones.</p><p><strong>Discussion: </strong>The association of an extensive leukoencephalopathy with an episodic memory dysfunction of the hippocampal type is strongly suggestive of a <i>LAMB1</i> end-truncating variation in adults older than 50 years. Early cognitive complaints and imaging abnormalities might exist decades before. Additional transient manifestations can be observed, and this association should lead to <i>LAMB1</i> screening to avoid unnecessary invasive investigations.</p>","PeriodicalId":48613,"journal":{"name":"Neurology-Genetics","volume":"9 3","pages":"e200069"},"PeriodicalIF":3.0000,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/4a/26/NXG-2023-000012.PMC10096279.pdf","citationCount":"0","resultStr":"{\"title\":\"Extension of the Clinicoradiologic Spectrum of Newly Described End-Truncating <i>LAMB1</i> Variations.\",\"authors\":\"Hélène Morel, Laurent Bailly, Cédric Urbanczyk, Dominique Hervé, Stéphane Berroir, Raphaël Le Bouc, Richard Levy, Mylène Meyer, Chaker Aloui, Elisabeth Tournier-Lasserve, Guillaume Mathey\",\"doi\":\"10.1212/NXG.0000000000200069\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>To refine the clinical spectrum of a very recently identified phenotype associated with <i>LAMB1</i> end-truncating pathogenic variations.</p><p><strong>Methods: </strong>Detailed clinical, neuropsychological, and MRI investigation of 6 patients from 2 unrelated families segregating end-truncating <i>LAMB1</i> variations.</p><p><strong>Results: </strong>All patients harbored <i>a LAMB1</i> end-truncating pathogenic variation. The specific association of a hippocampal type episodic memory dysfunction and a diffuse leukoencephalopathy was observed in all 4 patients aged older than 50 years, slightly worsening over time in 2 patients with several years of follow-up. Additional unspecific neurologic symptoms are reported, such as episodes of numbness, language troubles, or faintness in these 4 patients and the 2 younger ones.</p><p><strong>Discussion: </strong>The association of an extensive leukoencephalopathy with an episodic memory dysfunction of the hippocampal type is strongly suggestive of a <i>LAMB1</i> end-truncating variation in adults older than 50 years. Early cognitive complaints and imaging abnormalities might exist decades before. Additional transient manifestations can be observed, and this association should lead to <i>LAMB1</i> screening to avoid unnecessary invasive investigations.</p>\",\"PeriodicalId\":48613,\"journal\":{\"name\":\"Neurology-Genetics\",\"volume\":\"9 3\",\"pages\":\"e200069\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2023-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/4a/26/NXG-2023-000012.PMC10096279.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neurology-Genetics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1212/NXG.0000000000200069\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurology-Genetics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1212/NXG.0000000000200069","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
Extension of the Clinicoradiologic Spectrum of Newly Described End-Truncating LAMB1 Variations.
Objectives: To refine the clinical spectrum of a very recently identified phenotype associated with LAMB1 end-truncating pathogenic variations.
Methods: Detailed clinical, neuropsychological, and MRI investigation of 6 patients from 2 unrelated families segregating end-truncating LAMB1 variations.
Results: All patients harbored a LAMB1 end-truncating pathogenic variation. The specific association of a hippocampal type episodic memory dysfunction and a diffuse leukoencephalopathy was observed in all 4 patients aged older than 50 years, slightly worsening over time in 2 patients with several years of follow-up. Additional unspecific neurologic symptoms are reported, such as episodes of numbness, language troubles, or faintness in these 4 patients and the 2 younger ones.
Discussion: The association of an extensive leukoencephalopathy with an episodic memory dysfunction of the hippocampal type is strongly suggestive of a LAMB1 end-truncating variation in adults older than 50 years. Early cognitive complaints and imaging abnormalities might exist decades before. Additional transient manifestations can be observed, and this association should lead to LAMB1 screening to avoid unnecessary invasive investigations.
期刊介绍:
Neurology: Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. Original articles in all areas of neurogenetics will be published including rare and common genetic variation, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease-genes, and genetic variations with a putative link to diseases. This will include studies reporting on genetic disease risk and pharmacogenomics. In addition, Neurology: Genetics will publish results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology: Genetics, but studies using model systems for treatment trials are welcome, including well-powered studies reporting negative results.