Rothmund-Thomson syndrome type 3

Rothmund-Thomson syndrome type 3 is a rare condition that is also known by the names 'Rothmund-Thomson syndrome, type 3' and 'short stature with microcephaly and distinctive facies'. Limited detailed information is available about this condition. The condition has been catalogued in OMIM (OMIM:615789) and has been linked to the gene CRIPT.

Information about symptoms is currently limited for this condition.

There is an association with the gene CRIPT in people with this condition. However, further details regarding the causes and risk factors are currently limited.

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

Information about the outlook and long-term considerations for this condition is currently limited.

Current research and future directions for this condition are not well described in the available information.