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- Kocher–Debre–Semelaigne_syndrome abstract "The Kocher–Debré–Semelaigne syndrome is 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 Semelaigne.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.".
- Kocher–Debre–Semelaigne_syndrome wikiPageID "17455".
- Kocher–Debre–Semelaigne_syndrome wikiPageRevisionID "600846953".
- Kocher–Debre–Semelaigne_syndrome subject Category:Syndromes.
- Kocher–Debre–Semelaigne_syndrome comment "The Kocher–Debré–Semelaigne syndrome is hypothyroidism in infancy or childhood characterised by lower extremity or generalized muscular hypertrophy, myxoedema, short stature and cretinism.".
- Kocher–Debre–Semelaigne_syndrome label "Kocher–Debre–Semelaigne syndrome".
- Kocher–Debre–Semelaigne_syndrome label "Síndrome de Kocher".
- Kocher–Debre–Semelaigne_syndrome sameAs Kocher%E2%80%93Debre%E2%80%93Semelaigne_syndrome.
- Kocher–Debre–Semelaigne_syndrome sameAs Síndrome_de_Kocher.
- Kocher–Debre–Semelaigne_syndrome sameAs Q932899.
- Kocher–Debre–Semelaigne_syndrome sameAs Q932899.
- Kocher–Debre–Semelaigne_syndrome wasDerivedFrom Kocher–Debre–Semelaigne_syndrome?oldid=600846953.