What is another word for dennie-marfan syndrome?
Pronunciation: [dˈɛnimˈɑːfən sˈɪndɹə͡ʊm] (IPA) 
Dennie-Marfan syndrome is also known as Marfanoid habitus type D. It is a rare genetic disorder that is inherited in an autosomal dominant manner. This means that an affected person has a 50% chance of passing the condition to their offspring. There are no synonyms for Dennie-Marfan syndrome as it is named after the two doctors who first described it in 1958. The condition is characterized by the presence of long limbs, joint hypermobility, and a thin, elongated face. Other features of the condition may include cardiovascular abnormalities, skeletal abnormalities, and eye problems. It is important that individuals with Dennie-Marfan syndrome receive appropriate medical care and monitoring throughout their lives.
