LEOPARD syndrome 1

Any Noonan syndrome with multiple lentigines in which the cause of the disease is a heterozygous mutation in the PTPN11 gene on chromosome 12q24.

Also known as: LEOPARD syndrome 1, LEOPARD syndrome type 1, LPRD1, lentiginosis, cardiomyopathic, multiple lentigines syndrome

13 clinical trials for this condition and its sub-types, 0 tagged with LEOPARD syndrome 1 itself.