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[Heterochromia iridis, congenital deafness and skin pigmentary abnormalities: Waardenburg syndrome].

AuthorsNatalia Jiménez Gómez, M Asunción Ballester Martínez, Susana Urrutia Hernando, Pedro Jaén Olasolo
JournalMedicina clinica (Med Clin (Barc)) Vol. 142 Issue 6 Pg. e11 (Mar 20 2014) ISSN: 1578-8989 [Electronic] Spain
Vernacular TitleHeterocromía del iris, sordera congénita y alteraciones de la pigmentación cutánea: síndrome de Waardenburg.
PMID24029453 (Publication Type: Case Reports, Journal Article)
Topics
  • Adolescent
  • Cochlear Implantation
  • Deafness (genetics, surgery)
  • Early Diagnosis
  • Female
  • Hearing Loss, Sensorineural (genetics, surgery)
  • Humans
  • Hyperpigmentation (genetics)
  • Hypertelorism (genetics)
  • Iris Diseases (genetics)
  • Language Development Disorders (prevention & control)
  • Phenotype
  • Pigmentation Disorders (genetics)
  • Waardenburg Syndrome (diagnosis, genetics)

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