Monday, July 8, 2019

Molecular diagnostic workflow, clinical interpretation of sequence variants and data repository procedures in 140 individuals with familial cerebra... - PubMed - NCBI

Molecular diagnostic workflow, clinical interpretation of sequence variants and data repository procedures in 140 individuals with familial cerebra... - PubMed - NCBI



 2019 Jun 29. doi: 10.1002/humu.23851. [Epub ahead of print]

Molecular diagnostic workflow, clinical interpretation of sequence variants and data repository procedures in 140 individuals with familial cerebral cavernous malformations.

Abstract

Familial cerebral cavernous malformation (FCCM) is an autosomal dominant vascular disorder caused by heterozygous deleterious variants in KRIT1, CCM2 or PDCD10. In a previous study, we presented the clinical and molecular findings in 140 FCCM individuals. In the present work, we report supporting information on: (i) applied diagnostic workflow; (ii) clinical significance of molecular findings according to the American College of Medical Genetics and Genomics/Association for Molecular Pathology recommendations; (iii) standardization of molecular and clinical data according to the Human Phenotype Ontology; (iv) preliminary genotype-phenotype correlations on a subgroup of patients by considering sex, age at diagnosis, neurological symptoms, and number and anatomical site(s) of vascular anomalies; (v) datasets submitted to the Leiden Open Variation Database. An overview of the changes of our diagnostic approach before and after the transition to next generation sequencing is also reported. This work presents the full procedure that we apply for molecular testing, data interpretation and storing in public databases in FCCM. This article is protected by copyright. All rights reserved.

KEYWORDS:

CCM2; Human Phenotype Ontology; KRIT1; Leiden Open Variation Database; Mutation; PDCD10; variant interpretation

PMID:
 
31254430
 
DOI:
 
10.1002/humu.23851

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