Kocher-Debre-Semelaigne syndrome
From Wikipedia, the free encyclopedia
The Kocher-Debré-Semelaigne syndrome is a (myopathy) of hypothyroidism in infancy or childhood characterised by lower extremity or generalized muscular hypertrophy, myxoedema, short stature and cretinism. The absence of painful spasms and pseudomyotonia differentiates this syndrome from Hoffmann syndrome.
The syndrome is named after Emil Theodor Kocher, Robert Debré and Georges Semélaigne.
Also known as Debre-Semelaigne syndrome or cretinism-muscular hypertrophy, hypothyroid myopathy, hypothyroidism-large muscle syndrome, hypothyreotic muscular hypertrophy in children, infantile myxoedema-muscular hypertrophy, myopathy-myxoedema syndrome, myxoedema-muscular hypertrophy syndrome, myxoedema-myotonic dystrophy syndrome.
