Kocher-Debre-Semelaigne syndrome (Q106070): Difference between revisions

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Revision as of 12:51, 17 August 2026

This is a (myopathy) of hypothyroidism in infancy or childhood characterised by lower extremity or generalised muscular hypertrophy, myxoedema, short stature and cretinism.
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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