Noonan syndrome-like disorder with loose anagen hair 1

Noonan syndrome-like disorder with loose anagen hair 1 is a rare genetic condition that shares similarities with Noonan syndrome. It is also known by several names such as NSLH, NSLH1, and Tosti syndrome. This condition has been linked to changes in the SHOC2 gene, which plays a role in important cellular processes. Because the detailed definition and full range of features for this condition are not widely described in the available sources, information about the overall presentation remains limited. Research continues to improve understanding of how the genetic change in SHOC2 affects development and leads to the characteristic findings in people with this disorder.

Information about symptoms is currently limited for this condition.

Noonan syndrome-like disorder with loose anagen hair 1 is caused by a genetic change in the SHOC2 gene. This change can affect important cellular signaling pathways, which in turn may influence the way the body develops. Specific details about additional genetic risk factors or environmental influences are not available.

Information about treatment options and management approaches is currently limited for this condition.

Information about prognosis and quality of life for people with Noonan syndrome-like disorder with loose anagen hair 1 is currently limited for this condition.

Information about ongoing research and future directions for this condition is currently limited for this condition.