A 'Full House' Glomerulopathy in a Patient with Multiple Lentigines Syndrome: A Case Report
West Indian med. j; 67 (2), 2018
ABSTRACT Multiple lentigines syndrome (MLS) is an autosomal dominant disease which is usually diagnosed clinically by the presence of characteristic features. The molecular genetic testing is an adjuvant diagnostic tool to identify the mutation of particular genes such as PTPN11 genes, RAF1, BRAF or MAP2...