Journal of Oral Research (Oct 2022)

X-linked hypohidrotic ectodermal dysplasia management with removable prosthesis in a pediatric patient. Case Report.

  • Héctor Rodríguez,
  • José Rodríguez,
  • Maria Acosta de Camargo,
  • Hazel Topel,
  • Miguel Hirschhaut

DOI
https://doi.org/10.17126/joralres.2022.055
Journal volume & issue
Vol. 11, no. 5
pp. 1 – 8

Abstract

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Introduction: Ectodermal dysplasia is a rare genetic disorder that affects structures derived from ectoderm such as teeth, hair, nails, and sweat glands. Oligodontia is a common finding that affects the chewing, smiling and self- esteem of these pediatric patients. Case Report: We present a case report of a 7-years-old pediatric patient who consulted with his mother, showing the same condition. The intervention consisted of a removable prosthesis with satisfactory results. Conclusion: The X-linked hypohidrotic ectodermal dysplasia represents a challenge for a pediatric dentist who offers rehabilitation to the patient according to craniofacial development, age, socioeconomic status, and the number of missing teeth.

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