Uruguay Faciocardiomusculoskeletal syndrome

Uruguay Faciocardiomusculoskeletal syndrome is a rare condition that has been noted in medical records and research. It is known by several names including FCMSU, Fcms, and Uruguay type. Although a formal definition is not available, people with this condition have been associated with an X-linked recessive inheritance pattern. This syndrome has been linked to changes in the FHL1 gene. Documentation such as the OMIM entry (OMIM:300280) provides a reference point for further study and confirms the genetic association. The understanding of the full range of clinical features remains limited at this time.

Information about symptoms is currently limited for this condition.

The known cause of this syndrome is related to changes in the FHL1 gene. This gene is linked to the condition following an X-linked recessive pattern, which means that the inheritance and genetic risk follow specific patterns. Detailed information about other causes or risk factors is still limited.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

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