Pfeiffer syndrome type 3 (Q94911)

From determinar.ia.br - Determine suas informações
Revision as of 10:27, 16 August 2026 by Determinaradmin (talk | contribs) (‎Changed an Item)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Pfeiffer syndrome type 3 is a frequent severe type of Pfeiffer syndrome and is characterised by bicoronal craniosynostosis, severe associated functional disorders, and hand, foot and elbow abnormalities.
Language Label Description Also known as
default for all languages
ID_1910513449
    English
    Pfeiffer syndrome type 3
    Pfeiffer syndrome type 3 is a frequent severe type of Pfeiffer syndrome and is characterised by bicoronal craniosynostosis, severe associated functional disorders, and hand, foot and elbow abnormalities.

      Statements

      CID11:ID_1910513449
      0 references
      dki-india-ID_1910513449
      0 references
      Concluído
      0 references
      15 August 2026
      0 references