Noonan syndrome 5

Noonan syndrome 5 is a condition that is part of the Noonan syndrome group. It is defined by the presence of a mutation in the RAF1 gene. This condition shares features with other types of Noonan syndrome, but it is specifically linked to changes in RAF1. People with Noonan syndrome 5 may have overlapping features with other forms of Noonan syndrome, such as differences in heart structure and growth patterns. However, the defining factor for Noonan syndrome 5 is the mutation in the RAF1 gene, which distinguishes it from other types of Noonan syndrome.

Information about symptoms is currently limited for this condition.

Noonan syndrome 5 is caused by a mutation in the RAF1 gene. This genetic change affects cell signaling, which can influence growth and development. The mutation in RAF1 is the main factor that leads to the characteristics seen in this condition.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.