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Bilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1.

AuthorsPh Debeer, L Vandenbossche, T J L de Ravel, C Desloovere, L De Smet, C Huysmans, R Thoelen, J Vermeesch, W J M Van de Ven, J P Fryns
JournalClinical genetics (Clin Genet) Vol. 65 Issue 2 Pg. 153-5 (Feb 2004) ISSN: 0009-9163 [Print] Denmark
PMID14984476 (Publication Type: Case Reports, Letter)
Topics
  • Abnormalities, Multiple (diagnostic imaging, genetics)
  • Foot Deformities, Congenital (diagnostic imaging, genetics)
  • Hand Deformities, Congenital (diagnostic imaging, genetics)
  • Hearing Loss, Sensorineural (genetics)
  • Humans
  • Infant, Newborn
  • Male
  • Radiography
  • Radius (diagnostic imaging)
  • Synostosis (diagnostic imaging, genetics)
  • Ulna (diagnostic imaging)

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