Noonan syndrome 10

Noonan syndrome 10 is a form of Noonan syndrome caused by a mutation in the LZTR1 gene. This condition is part of a group of disorders that affect growth, development, and other body systems. The condition falls under the broader category of Noonan syndromes but is specifically linked to changes in the LZTR1 gene. People with this condition may experience features that are part of Noonan syndrome. However, detailed information on the full spectrum of physical manifestations and variability among affected individuals is limited based on the available sources.

Information about symptoms is currently limited for this condition.

The cause of Noonan syndrome 10 is a mutation in the LZTR1 gene. This genetic alteration leads to changes in the structure or function of the LZTR1 protein, which plays a role in various cellular processes. As a genetic condition, it is inherited in a pattern associated with changes in this specific gene.

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.