The focal facial dermal dysplasias: phenotypic spectrum and molecular genetic heterogeneity

J Med Genet. 2017 Sep;54(9):585-590. doi: 10.1136/jmedgenet-2017-104561. Epub 2017 Jun 29.

Abstract

Focal facial dermal dysplasias (FFDDs) are rare genetic/developmental disorders characterised by bilateral 'scar-like' facial lesions. Four subtypes are classified by the bitemporal (FFDD1-3) or preauricular (FFDD4) lesion location. FFDD1-3 are differentiated by additional facial abnormalities and inheritance patterns. Although the genetic defects causing FFDD1 and FFDD2 remain unknown, recent studies identified defects causing FFDD3 and FFDD4. Here, the clinical phenotypes, genetic defects and inheritance of the four FFDD subtypes are described. In addition, the overlapping facial abnormalities in FFDD3 and two other genetic disorders, Ablepharon macrostomia syndrome and Barber-Say syndrome, are noted. Familiarity with the FFDDs by clinicians will further delineate the phenotypes and genetic/developmental defects of these dermal facial disorders.

Keywords: Barber-Say syndrome; TWIST2; ablepharon-macrostomia syndrome; chromosome 1p36; focal facial dermal dysplasia.

Publication types

  • Review

MeSH terms

  • Ectodermal Dysplasia / genetics*
  • Face / abnormalities*
  • Female
  • Focal Dermal Hypoplasia / genetics*
  • Focal Facial Dermal Dysplasias
  • Genetic Heterogeneity
  • Humans
  • Male
  • Phenotype
  • Skin Diseases / genetics*