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Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder.
Haensel, Jennifer; Kohlschmidt, Nicolai; Pitz, Susanne; Keilmann, Annerose; Zenker, Martin; Ullmann, Reinhard; Haaf, Thomas; Bartsch, Oliver.
Affiliation
  • Haensel J; Institute of Human Genetics, Johannes Gutenberg University, Mainz, Germany.
Am J Med Genet A ; 149A(10): 2236-40, 2009 Oct.
Article in En | MEDLINE | ID: mdl-19760652
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Eyelids / Macrostomia Type of study: Diagnostic_studies Limits: Child / Female / Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2009 Document type: Article Affiliation country: Alemania

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Eyelids / Macrostomia Type of study: Diagnostic_studies Limits: Child / Female / Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2009 Document type: Article Affiliation country: Alemania
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