摘要
One of the autosomal dominant tissue disorders is Marfan syndrome that affects different organ systems.Mainly,Marfan syndrome causing abnormalities in the heart,blood vessels,eyes,bones,and joints.Most Often,features of Marfan syndrome are vision problems,defects in the large blood vessel-like aorta,tall and very thin,have long fingers and toes(arachnodactyly),and have an arm span exceeding the height of their body.Moreover,Other common features include a long and narrow face,crowded teeth,and scoliosis,or kyphosis.We presented a thirty-three years old female known case of Systemic Lupus erythematosus(SLE)and had Marfan syndrome,presented to the emergency department with complaints of headache and fever for two days.The patient denied any complaining of vomiting,blurred vision,dizziness.
基金
The authors acknowledge the patient who consented to publish this report and acknowledge the neuro and orthopedic staff at Sultan Qaboos University for their support and collaboration。
