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Another case of preaxial polydactyly and white forelock in branchio-oculo-facial syndrome.

Abstract
A 1-year-old male with branchio-oculo-facial syndrome together with preaxial polydatyly and a white forelock at birth is described. This is only the second case where preaxial polydactyly has been described in branchio-oculo-facial syndrome. In both cases a diagnosis of Waardenburg syndrome had been considered.
AuthorsJ McGaughran
JournalClinical dysmorphology (Clin Dysmorphol) Vol. 10 Issue 1 Pg. 67-8 (Jan 2001) ISSN: 0962-8827 [Print] England
PMID11152153 (Publication Type: Case Reports, Letter)
Topics
  • Branchio-Oto-Renal Syndrome (diagnosis)
  • Humans
  • India (ethnology)
  • Infant
  • Male
  • New Zealand
  • Piebaldism
  • Polydactyly (diagnosis)
  • Skin Abnormalities (diagnosis)

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