Cornelia de Lange syndrome 5

Cornelia de Lange syndrome 5 is a rare genetic condition that is one form within the spectrum of Cornelia de Lange syndromes. This condition has been associated with changes in the HDAC8 gene and is also known by several other names such as Cornelia De Lange syndrome type 5, CDLS5, and X-linked dominant Cornelia de Lange syndrome 5. While detailed information describing the features and overall clinical presentation is limited, the condition is recognized in genetic databases including OMIM and GARD. The available identifiers help healthcare professionals track and study this disorder further, even though comprehensive descriptions about its presentation are not currently available.

Information about symptoms is currently limited for this condition.

Research has noted that alterations in the HDAC8 gene are associated with Cornelia de Lange syndrome 5. However, detailed information regarding other genetic causes or risk factors is currently limited for 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.