A rare condition: Larsen Syndrome

• 作者: Abdalla Alshdaifat Abdu Mueed Bidchol Aisha Alshdefat Harshita Prabhakaran
• 来源期刊: TMR整合护理
• 学科: 医学
• 关键词: Larsen Syndrome INHERITED NEWBORN distinct disease
• 年，卷（期）: 2020,（6）
• 页码范围: 215-218
• 页数: 4页
• 分类号: R73

摘要

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.