1. Academic Validation
  2. Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder

Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder

  • Am J Med Genet A. 2009 Oct;149A(10):2236-40. doi: 10.1002/ajmg.a.32993.
Jennifer Haensel 1 Nicolai Kohlschmidt Susanne Pitz Annerose Keilmann Martin Zenker Reinhard Ullmann Thomas Haaf Oliver Bartsch
Affiliations

Affiliation

  • 1 Institute of Human Genetics, Johannes Gutenberg University, Mainz, Germany.
Abstract

We report on a 7-year-old girl with unequivocal features of Barber-Say syndrome (BSS): generalized hypertrichosis especially at the back, dry lax skin, macrostomia, thin lips, cup-shaped ears, bulbous nose, hypoplastic nipples, and abnormal external genitalia. She also demonstrated conductive hearing impairment and microblepharon. BSS has been reported with ectropion (not present in our patient), but ablepharon and microblepharon (i.e., absent or hypoplastic eyelids) have always been considered as hallmarks of ablepharon macrostomia syndrome (AMS). This is the first report of microblepharon in BSS. Other authors have discussed that BSS and AMS could possibly represent one syndrome, and our report supports this hypothesis.

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