Larsen Syndrome is a rare inherited severe disease that described for the first time in the medical field as a distinct disease by Dr.Loren Larsen in 1950.It is characterized by congenital dislocation of multiple join...Larsen Syndrome is a rare inherited severe disease that described for the first time in the medical field as a distinct disease by Dr.Loren Larsen in 1950.It is characterized by congenital dislocation of multiple joints along with other anomalies,including heart,face,hands,and bones.We present a two years five months male who presented with facial dysmorphic features like low set of ears,depressed nasal bridge,micro-retrognathia,and broad forehead.展开更多
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 ...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.展开更多
文摘Larsen Syndrome is a rare inherited severe disease that described for the first time in the medical field as a distinct disease by Dr.Loren Larsen in 1950.It is characterized by congenital dislocation of multiple joints along with other anomalies,including heart,face,hands,and bones.We present a two years five months male who presented with facial dysmorphic features like low set of ears,depressed nasal bridge,micro-retrognathia,and broad forehead.
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。
文摘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.
