Novel MBTPS2 Missense Mutation in the N-Terminus Transmembrane Domain in a Patient with Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome

作者：Izumi Kosuke^*; Wilkens Alisha; Treat James R; Pride Howard B; Krantz Ian D

来源：Pediatric Dermatology, 2013, 30(6): E263-E264.

DOI：10.1111/pde.12115

Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome is an X-linked dominant condition characterized by the triad of ichthyosis follicularis, alopecia, and photophobia caused by mutations in the MBTPS2 gene. Herein we describe a proband with IFAP syndrome with mild cutaneous manifestations and a novel MBTPS2 mutation in the N-terminal transmembrane domain.

• 出版日期2013-11