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A rare condition: Larsen Syndrome
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作者 Aisha Alshdefat Abdu Mueed Bidchol +1 位作者 harshita prabhakaran Abdalla Alshdaifat 《TMR Integrative Nursing》 2020年第6期215-218,共4页
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
关键词 Larsen Syndrome INHERITED NEWBORN distinct disease
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