Marfan Syndrome with Systemic Lupus erythematosus  

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作  者:Aisha Alshdefat Abdu Mueed Bidchol Abdalla Alshdaifat Rasha Abu Baker 

机构地区:[1]Department of Maternal and Child Health,College of Nursing,Sultan Qaboos University,Sultanate of Oman [2]Genetic Reporting Manager,Al Ward Medical Services,Sultanate of Oman [3]Medical Student,University of Lodz,Republic of Poland [4]不详

出  处:《TMR Integrative Nursing》2020年第5期172-175,共4页TMR整合护理

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。

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.

关 键 词:Marfan Syndrome autosomal subdural subacute on chronic hemorrhage Systemic Lupus erythematosus 

分 类 号:R59[医药卫生—内科学]

 

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