Warning: The NCBI web site requires JavaScript to function. more...
Generate a file for use with external citation management software.
In seven consecutive melanoma-prone families, pigmented lesions with distinctive clinical and histologic characteristics occurred in 18 of 20 melanoma patients (90%) and 24 of 43 first-degree relatives (56%). Recognition of these lesions led to the detection of early-stage melanoma in six family members. This syndrome appears to represent an autosomal dominant trait and may serve as a cutaneous marker to identify persons at high risk for melanoma.
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on