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http://purl.uniprot.org/citations/12877753http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12877753http://www.w3.org/2000/01/rdf-schema#comment"

Background

Cerebral cavernous malformations (CCM) present as either sporadic or autosomal dominant conditions with incomplete penetrance of symptoms. Differences in genetic and environmental factors might be minimized among first-degree relatives. We therefore studied clinical expression in a family with several affected members.

Methods

We studied a three-generation family with the onset of CCM as a cerebral haemorrhage in the younger (four-year-old) sibling. Identification and enumeration of CCMs were performed in T2-weighted or gradient-echo MRIs of the whole brains. Genetic analysis comprised SCCP, sequencing and restriction polymorphism of the Krit1 gene in the proband and at risk relatives.

Results

The phenotypes of cerebral cavernous malformations (CCMs) in carriers of Krit1 mutations were very variable. We identified a novel frameshift mutation caused by a 1902A insertion in exon 17 of the Krit1 gene, which leads to a premature TAA triplet and predicts the truncating phenotype Y634X. A very striking finding was the absence of both clinical symptoms and CCMs in the eldest sibling harbouring the 1902insA.

Conclusions

Patients in this family, harbouring the same mutation, illustrate the very variable clinical and radiological expression of a Krit1 mutation. The early and critical onset in the proband contrasts with minor clinical findings in affected relatives. This consideration is important in genetic counselling."xsd:string
http://purl.uniprot.org/citations/12877753http://purl.org/dc/terms/identifier"doi:10.1186/1471-2377-3-5"xsd:string
http://purl.uniprot.org/citations/12877753http://purl.uniprot.org/core/author"Lucas M."xsd:string
http://purl.uniprot.org/citations/12877753http://purl.uniprot.org/core/author"Costa A.F."xsd:string
http://purl.uniprot.org/citations/12877753http://purl.uniprot.org/core/author"Solano F."xsd:string
http://purl.uniprot.org/citations/12877753http://purl.uniprot.org/core/author"Izquierdo G."xsd:string
http://purl.uniprot.org/citations/12877753http://purl.uniprot.org/core/author"Gamero M.A."xsd:string
http://purl.uniprot.org/citations/12877753http://purl.uniprot.org/core/author"Garcia-Moreno J.M."xsd:string
http://purl.uniprot.org/citations/12877753http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/12877753http://purl.uniprot.org/core/name"BMC Neurol"xsd:string
http://purl.uniprot.org/citations/12877753http://purl.uniprot.org/core/pages"5"xsd:string
http://purl.uniprot.org/citations/12877753http://purl.uniprot.org/core/title"Variable expression of cerebral cavernous malformations in carriers of a premature termination codon in exon 17 of the Krit1 gene."xsd:string
http://purl.uniprot.org/citations/12877753http://purl.uniprot.org/core/volume"3"xsd:string
http://purl.uniprot.org/citations/12877753http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/12877753
http://purl.uniprot.org/citations/12877753http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/12877753
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http://purl.uniprot.org/uniprot/A0A0C4DG23http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/12877753