CHAND syndrome

CHAND syndrome, also known as CHANDS or curly hair-ankyloblepharon-nail dysplasia syndrome, is a rare condition. The condition is identified by its unique combination of features suggested by its name, although detailed clinical information is limited in the available sources. Identifiers from trusted resources such as OMIM, Orphanet, and GARD highlight this condition in the medical literature.

Information about symptoms is currently limited for this condition.

The known genetic factor in CHAND syndrome is related to the RIPK4 gene. Current available evidence indicates that mutations in this gene are associated with the condition. More detailed information about genetic causes and risk factors is not available from the provided sources.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

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