GAPO Syndrome-A Rare Cause of Osteomyelitis of Jaws; Report of 4 Cases With a Brief Review of the Literature

J Oral Maxillofac Surg. 2018 Jun;76(6):1216-1225. doi: 10.1016/j.joms.2017.12.002. Epub 2017 Dec 12.

Abstract

GAPO syndrome is characterized by growth retardation, alopecia, pseudoanodontia, and ophthalmic abnormalities. This very rarely reported syndrome affects various ethnic groups and can present with manifestations other than those usually reported. Pseudoanodontia is a rare clinical and radiologic manifestation that is always associated with GAPO syndrome. Osteomyelitis of the jaws is a less common disease that is usually attributed to odontogenic causes. This case report describes osteomyelitis of the mandible in a patient with GAPO syndrome. Further, an additional 3 cases of GAPO in the patient's family, with special emphasis on oral mucosal changes and pseudoanodontia, are discussed.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Alopecia / complications*
  • Alopecia / genetics
  • Anodontia / complications*
  • Anodontia / genetics
  • Child
  • Child, Preschool
  • Consanguinity
  • Female
  • Growth Disorders / complications*
  • Growth Disorders / genetics
  • Humans
  • India
  • Jaw Diseases / diagnostic imaging
  • Jaw Diseases / etiology*
  • Male
  • Optic Atrophies, Hereditary / complications*
  • Optic Atrophies, Hereditary / genetics
  • Osteomyelitis / diagnostic imaging
  • Osteomyelitis / etiology*
  • Pedigree

Supplementary concepts

  • Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy