Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

BACKGROUND: Multiple cutaneous and uterine leiomyomata syndrome (MCUL; MIM 150800) is a rare condition that sometimes predisposes to renal cancer. It is caused by deleterious mutations in the fumarate hydratase (FH) gene. In many patients, skin leiomyomas have been reported to develop according to a segmental type 1 or type 2 distribution. We report a patient showing multiple leiomyomas distributed according to a segmental type 2 distribution and covering several areas exclusively on the left side of his body. OBJECTIVE: To search for a specific mutation in the FH gene associated with this phenotype. METHODS: Genomic DNA from peripheral blood leucocytes of the proband was sequenced and screened for mutation of the FH gene. RESULTS: Heterozygosity for an as yet undescribed mutation c.695delG, leading to a truncated protein p.Gly232AspfsX24, was found. CONCLUSION: We report a new mutation in the FH gene and discuss the unusual pattern of purely unilateral distribution in the present case.

Original publication




Journal article



Publication Date





149 - 153


Adult, Fumarate Hydratase, Genetic Predisposition to Disease, Humans, Laser Therapy, Leiomyomatosis, Male, Neoplastic Syndromes, Hereditary, Sequence Deletion, Skin Neoplasms, Treatment Outcome, Uterine Neoplasms