Absence of Fingerprints-Congenital Milia Syndrome

Absence of Fingerprints-Congenital Milia Syndrome, also known as absence of dermatoglyphics-congenital milia syndrome, is related to basan syndrome. An important gene associated with Absence of Fingerprints-Congenital Milia Syndrome is SMARCAD1 (SWI/SNF-Related, Matrix-Associated Actin-Dependent Regulator Of Chromatin, Subfamily A, Containing DEAD/H Box 1). Affiliated tissues include skin, and related phenotypes are abnormal dermatoglyphics and abnormal blistering of the skin