Three cases of CATCH 22 syndrome with cleft palate.

  • TANAKA Noriaki
    First Department of Oral and Maxillofacial Surgery, Division of Pathogenesis and Control of Oral Disease, Course for Integrated Oral Sciences and Stomatology, Osaka University
  • IIDA Seiji
    First Department of Oral and Maxillofacial Surgery, Division of Pathogenesis and Control of Oral Disease, Course for Integrated Oral Sciences and Stomatology, Osaka University
  • KOGO Mikihiko
    First Department of Oral and Maxillofacial Surgery, Division of Pathogenesis and Control of Oral Disease, Course for Integrated Oral Sciences and Stomatology, Osaka University
  • ISHII Syouichirou
    First Department of Oral and Maxillofacial Surgery, Division of Pathogenesis and Control of Oral Disease, Course for Integrated Oral Sciences and Stomatology, Osaka University
  • SENOO Hitomi
    First Department of Oral and Maxillofacial Surgery, Division of Pathogenesis and Control of Oral Disease, Course for Integrated Oral Sciences and Stomatology, Osaka University
  • URABE Kazuhiko
    First Department of Oral and Maxillofacial Surgery, Division of Pathogenesis and Control of Oral Disease, Course for Integrated Oral Sciences and Stomatology, Osaka University
  • MATSUYA Tokuzo
    First Department of Oral and Maxillofacial Surgery, Division of Pathogenesis and Control of Oral Disease, Course for Integrated Oral Sciences and Stomatology, Osaka University

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Other Title
  • 軟口蓋裂を伴ったCATCH22症候群の3例

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Description

CATCH 22 syndrome, defined by Wilson in 1993, is associated with cardiac defects, abnormal face, thymic hypoplasia, cleft palate, and hypocalcemia resulting from microdeletions of chromosome 22q11. We report three cases of CATCH 22 syndrome with cleft palate. All patients had a small mouth, bloated eye lids, and a low nasal bridge. Ocular hypertelorism and short palpebral fissures were found in two patients. Two had tetralogy of fallot, and none had thymic hypoplasia. Palatoplasty was performed in all three patients.

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