📂 Diseases
Larsen syndrome — Definition
Larsen sendromu / Larsen syndrome
Larsen syndrome is a rare genetic disease characterized by joint dislocations, facial anomalies and skeleton system disorders. Usually in the joints of knee, hip and elbow are accompanied by findings such as innate outs, straightened facial appearance, hypertelorism (wide range eyes) and palate half. Otozomal can show dominant or resesif inheritance paterni and is associated with mutations in the FLNB gene.
Frequently Asked Questions
❓ What is Larsen sendromu?
Larsen sendromu; larsen syndrome is a rare genetic disease characterized by joint dislocations, facial anomalies and skeleton system disorders. Usually in the joints of knee, hip and elbow are accompanied by findings such as innate outs, straightened facial appearance, hypertelorism (wide range eyes) and palate half. Otozomal can show dominant or resesif inheritance paterni and is associated with mutations in the FLNB gene.
❓ What is Larsen syndrome in Turkish?
The Turkish equivalent of "Larsen syndrome" is Larsen sendromu.
❓ Which medical field is Larsen sendromu related to?
This term belongs to the Diseases category.