{"id":21378,"date":"2023-02-22T14:49:34","date_gmt":"2023-02-22T14:49:34","guid":{"rendered":"https:\/\/www.sc101.org\/?page_id=21378"},"modified":"2023-02-24T20:02:24","modified_gmt":"2023-02-24T20:02:24","slug":"stroke","status":"publish","type":"page","link":"https:\/\/www.sc101.org\/sicklepedia\/stroke\/","title":{"rendered":"Stroke"},"content":{"rendered":"\n
Stroke and cognitive problems are the most common permanent complications of sickle cell disease.1\u00a0\u00a0 Historically 10% of people who had sickle cell disease had a stoke by the time they were 20 years old.\u00a0 Most of those strokes occurred between the age of 6 and 10 years.\u00a0 There was no predictor for stroke they could occur during a severe acute problem such as acute chest syndrome and they could also occur in children who were do relatively well without any warning.\u00a0\u00a0By the age of 40 years 20% of people who had sickle cell anemia (SS) had suffered a stroke and 10% of those suffering from SC disease had a stroke.\u00a0\u00a0In a study at Howard University 4% of children who suffered a stroke died and in a California study 7% of stroke victims with a stroke died2.\u00a0\u00a0Children who have sickle cell disease have about 200 times the risk of stroke compared to children who do not have sickle cell disease.<\/p>\n\n\n\n