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Pediatric Cerebral Arachnoid Cysts are Genetically-Encoded Harbingers of Neurodevelopmental Pathology.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Pediatric Cerebral Arachnoid Cysts are Genetically-Encoded Harbingers of Neurodevelopmental Pathology./
作者:
Allington, Garrett.
面頁冊數:
1 online resource (190 pages)
附註:
Source: Dissertations Abstracts International, Volume: 85-01, Section: B.
Contained By:
Dissertations Abstracts International85-01B.
標題:
Genetics. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30312493click for full text (PQDT)
ISBN:
9798379781453
Pediatric Cerebral Arachnoid Cysts are Genetically-Encoded Harbingers of Neurodevelopmental Pathology.
Allington, Garrett.
Pediatric Cerebral Arachnoid Cysts are Genetically-Encoded Harbingers of Neurodevelopmental Pathology.
- 1 online resource (190 pages)
Source: Dissertations Abstracts International, Volume: 85-01, Section: B.
Thesis (Ph.D.)--Yale University, 2023.
Includes bibliographical references
Cerebral arachnoid cysts (ACs) are among the most common human developmental brain lesions, yet, because ACs are not possible to reliably model in lower mammals, the pathogenic mechanisms driving AC formation remain poorly understood. To begin to elucidate AC pathogenesis, we performed an integrated analysis of 617 proband-parent exome trios, 152,898 brain and meningeal single-cell transcriptomes, and artificially-intelligent natural language processor data of proband medical records. We found damaging de novo variants (DNVs) were highly enriched in AC probands versus controls (P = 1 .57 x 10-33). Seven genes harbored an exome-wide significant DNV burden. AC-associated genes are enriched for chromatin modifiers and converged in midgestational transcription networks essential for neural and meningeal development. Unsupervised clustering of patient phenotypes identified four AC subtypes and clinical severity correlated with the presence of a damaging DNV. These results shed unique insight into the coordinated regulation of brain and meningeal development and implicate epigenomic dysregulation due to protein-damaging DNVs in AC pathogenesis, suggesting associated neurodevelopmental phenomena in the context of AC may be largely unrelated to mass effect, but rather due to an underlying common defect in early neurodevelopment. In the appropriate clinical context, ACs may be considered radiographic harbingers of neurodevelopmental pathology warranting additional genetic testing and neurobehavioral follow-up. These data also highlight the utility of a systems-level, multi-omics approach to elucidate sporadic structural brain disease, describing novel methodologies which may be broadly-applicable to the further study of a variety of pediatric neurological defects.
Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2023
Mode of access: World Wide Web
ISBN: 9798379781453Subjects--Topical Terms:
530508
Genetics.
Subjects--Index Terms:
Arachnoid membraneIndex Terms--Genre/Form:
542853
Electronic books.
Pediatric Cerebral Arachnoid Cysts are Genetically-Encoded Harbingers of Neurodevelopmental Pathology.
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Cerebral arachnoid cysts (ACs) are among the most common human developmental brain lesions, yet, because ACs are not possible to reliably model in lower mammals, the pathogenic mechanisms driving AC formation remain poorly understood. To begin to elucidate AC pathogenesis, we performed an integrated analysis of 617 proband-parent exome trios, 152,898 brain and meningeal single-cell transcriptomes, and artificially-intelligent natural language processor data of proband medical records. We found damaging de novo variants (DNVs) were highly enriched in AC probands versus controls (P = 1 .57 x 10-33). Seven genes harbored an exome-wide significant DNV burden. AC-associated genes are enriched for chromatin modifiers and converged in midgestational transcription networks essential for neural and meningeal development. Unsupervised clustering of patient phenotypes identified four AC subtypes and clinical severity correlated with the presence of a damaging DNV. These results shed unique insight into the coordinated regulation of brain and meningeal development and implicate epigenomic dysregulation due to protein-damaging DNVs in AC pathogenesis, suggesting associated neurodevelopmental phenomena in the context of AC may be largely unrelated to mass effect, but rather due to an underlying common defect in early neurodevelopment. In the appropriate clinical context, ACs may be considered radiographic harbingers of neurodevelopmental pathology warranting additional genetic testing and neurobehavioral follow-up. These data also highlight the utility of a systems-level, multi-omics approach to elucidate sporadic structural brain disease, describing novel methodologies which may be broadly-applicable to the further study of a variety of pediatric neurological defects.
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