Kocher-Debre-Semelaigne syndrome (Q106070)

From determinar.ia.br - Determine suas informações
Revision as of 12:51, 17 August 2026 by Determinaradmin (talk | contribs) (‎Changed an Item)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
This is a (myopathy) of hypothyroidism in infancy or childhood characterised by lower extremity or generalised muscular hypertrophy, myxoedema, short stature and cretinism.
Language Label Description Also known as
default for all languages
ID_109007822
    English
    Kocher-Debre-Semelaigne syndrome
    This is a (myopathy) of hypothyroidism in infancy or childhood characterised by lower extremity or generalised muscular hypertrophy, myxoedema, short stature and cretinism.

      Statements

      CID11:ID_109007822
      0 references
      dki-india-ID_109007822
      0 references
      Concluído
      0 references
      16 August 2026
      0 references