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Discovery of familial cerebral cavernous malformation in a Saudi population
  1. Shahpar Nahrir1,
  2. Majed H Al-Hameed1,
  3. Omar A Al-Sinaidi1,
  4. Wafa Al Shakweer2
  1. 1Department of Neurology, NNI, Riyadh, Saudi Arabia
  2. 2Department of Pathology, King Fahad Medical City, Riyadh, Saudi Arabia
  1. Correspondence to Dr Shahpar Nahrir, s_nahrir{at}


Familial cerebral cavernous malformation is a rare entity. It has been described commonly among the Hispanic population and sparsely among the Italian, French, Swedish and Chinese populations. We discovered two families with this condition among the Saudi population for the first time. Both the index patients had a seizure as a prominent manifestation of their underlying structural lesion. One of them had recurrent attacks of bleeding in the cavernoma leading to a focal neurological deficit. The siblings and the parents of both the patients were screened using CT of the brain imaging. Two members within each family were found to have symptomatic cavernoma. A molecular genetics study revealed heterozygous KRIT1/CCM1 for a frameshift mutation in one of the patients. No detectable mutation was found in the other patient. These cases illustrate the existence of this condition beyond the commonly known geographical area of higher prevalence. Moreover, KRIT1/CCM1 might be the possible target gene that is mutated in this region.

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