Infantile cortical hyperostosis (Q98922)

From determinar.ia.br - Determine suas informações
Revision as of 15:34, 16 August 2026 by Determinaradmin (talk | contribs) (‎Changed an Item)
Infantile cortical hyperostosis or Caffey disease is a rare condition which presents most commonly in infants who present with irritability, pain, tenderness, hyperaesthesia, soft tissue swelling and redness involving one or several areas of the body. Systemic changes with fever are usually present in the early stages. The pain may be severe enough to result in pseudoparalysis and individual nerve involvement may result in true localised palsies. Other reported clinical findings include dysphagia and nasal obstruction.
Language Label Description Also known as
default for all languages
ID_284169445
    English
    Infantile cortical hyperostosis
    Infantile cortical hyperostosis or Caffey disease is a rare condition which presents most commonly in infants who present with irritability, pain, tenderness, hyperaesthesia, soft tissue swelling and redness involving one or several areas of the body. Systemic changes with fever are usually present in the early stages. The pain may be severe enough to result in pseudoparalysis and individual nerve involvement may result in true localised palsies. Other reported clinical findings include dysphagia and nasal obstruction.

      Statements

      CID11:ID_284169445
      0 references