Kocher-Debre-Semelaigne syndrome

WordNet

1. a pattern of symptoms indicative of some disease
2. a complex of concurrent things; "every word has a syndrome of meanings"
3. German bacteriologist who isolated the anthrax bacillus and the tubercle bacillus and the cholera bacillus (1843-1910) (同)Robert_Koch

PrepTutorEJDIC

1. (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態

Wikipedia preview

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/07/12 14:24:20」(JST)

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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.

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• 1. 甲状腺機能低下性ミオパチー hypothyroid myopathy
• 2. 筋力低下を呈する小児の病因および評価 etiology and evaluation of the child with muscle weakness

English Journal

• Kocher-Debre-Semelaigne syndrome with arrhythmogenic right ventricular cardiomyopathy: A hitherto unrecognized association.

• Moorthy N, Kumar S, Dabadghao P, Kapoor A.SourceDepartment of Cardiology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
• Indian journal of endocrinology and metabolism.Indian J Endocrinol Metab.2012 Nov;16(6):1032-4. doi: 10.4103/2230-8210.103034.
• Kocher-Debre-Semelaigne (KDS) syndrome is a rare form of hypothyroid myopathy, with associated hypertrophy of muscles. Although cardiac manifestations of hypothyroidism are well known, reports of cardiac involvement in KDS have only described the occurrence of pericardial effusion as an association.
• PMID 23226660

Japanese Journal

• Kocher Debre Semelaigne syndrome and associated orofacial aspects: report of a case

• Patney Aditya,Pai Keerthilatha M.,Sholapurkar Amar A.
• Journal of Oral Science 53(1), 129-132, 2011
• … Myopathy and muscular pseudohypertrophy associated with severe congenital hypothyroidism has been described as Kocher Debre Semelaigne syndrome, which is a rare disorder with only a few previously published reports. … However, none of these reports have described the orofacial aspects of this syndrome. …
• NAID 130000659047

Related Links

• Rare disease: Kocher–Debré–Semelaigne syndrome

This combination of hypothyroidism and hypertrophy of muscles is classically described as Kocher–Debré–Semelaigne syndrome. This child was started on 50 µg of levothyroxine. Background Though it is a rare condition, the ...

• Kocher-Debre-Semelaigne syndrome - Medical Dictionary

Ko·cher-De·bré-Sé·mé·laigne syn·drome (kō'kĕr dĕ-brā' sā-mā-lān'), autosomal recessive inherited athyrotic cretinism associated with muscular pseudohypertrophy. Synonym(s): Debré-Sémélaigne syndrome Debré, Robert, French ...

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★リンクテーブル★

リンク元	「コシェル・ドゥブレ・セメレーニュ症候群」
関連記事	「syndrome」

「コシェル・ドゥブレ・セメレーニュ症候群」

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英

Kocher Debre Semelaigne syndrome, Kocher-Debre-Semelaigne syndrome, KDS syndrome

関

ホフマン症候群

「syndrome」

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• n.

• 症候群