1. Predictive genetic testing of at-risk relatives requires analysis of all CCM genes after identification of an unclassified CCM1 variant in an individual affected with cerebral cavernous malformations
- Author
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Stefanie Spiegler, Winnie Schröder, Ute Felbor, Juliane Najm, Wolfram Henn, Julio Viera, and Martina Mair
- Subjects
Hemangioma, Cavernous, Central Nervous System ,DNA Mutational Analysis ,Mutation, Missense ,Risk Assessment ,Cerebral cavernous malformations ,Predictive Value of Tests ,Proto-Oncogene Proteins ,Humans ,Medicine ,Missense mutation ,Genetic Testing ,Predictive testing ,KRIT1 Protein ,Gene ,Genetic testing ,Genetics ,medicine.diagnostic_test ,business.industry ,Genetic Variation ,Membrane Proteins ,General Medicine ,Middle Aged ,Cavernous malformations ,medicine.disease ,Magnetic Resonance Imaging ,Mutation (genetic algorithm) ,Female ,Surgery ,Identification (biology) ,Neurology (clinical) ,Apoptosis Regulatory Proteins ,Carrier Proteins ,business ,Microtubule-Associated Proteins - Abstract
The mutation detection rate for familial cerebral cavernous malformations (CCM) is extremely high, being about 90 % if direct sequencing of the three genes, CCM1, CCM2, and CCM3, is used in conjunction with quantitative analyses to detect larger CCM1-3 deletions/duplications. We here report on an individual who had presented with more than 30 cerebral and spinal cavernous malformations, two intracranial meningiomas, and disease manifestation only in the mid-forties. A CCM1 missense variant of unclear relevance was found during the first sequencing step. Thereafter, direct sequencing of all three CCM genes revealed the typical pathogenic loss-of-function mutation c.598C > T/p.Q200* in the CCM3 gene. Our results demonstrate that mutation analyses of all three CCM genes in the index patient regardless of previous identification of an unclassified CCM1 variant is crucial for reliable predictive testing of at-risk relatives.
- Published
- 2013
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