neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities

Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities is a rare genetic condition. It is known by its distinctive name and is linked to a change in the KDM6B gene. This condition has been catalogued in databases such as OMIM (ID: OMIM:618505). Detailed information about the overall features and progression of the condition is still limited.

Information about symptoms is currently limited for this condition.

This condition has been associated with changes in the KDM6B gene. However, more detailed information regarding the exact genetic causes and risk factors is currently limited.

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

Information about the outlook and quality of life for people with this condition is currently limited.

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