Toriello-Lacassie-Droste syndrome

Toriello-Lacassie-Droste syndrome, also known as oculo-ectodermal syndrome, is a rare condition that is primarily defined by the presence of epibulbar dermoids and aplasia cutis congenita. Epibulbar dermoids are benign growths on the eye, and aplasia cutis congenita refers to areas where skin does not develop normally at birth. This condition has been recognized under several different names, reflecting its association with the eye and skin findings.

People with this condition commonly have epibulbar dermoids, which are benign skin-like lesions on or around the eye, along with aplasia cutis congenita, where patches of skin are absent at birth. These symptoms are the main findings that help in understanding the condition.

The condition has been associated with the KRAS gene. The specific changes or mutations in this gene may play a role in the development of the syndrome. However, detailed information about genetic causes and risk factors is limited.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

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