WordNet

a pattern of symptoms indicative of some disease
a complex of concurrent things; "every word has a syndrome of meanings"
the 18th letter of the Roman alphabet (同)r

PrepTutorEJDIC

(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
resistance / 17歳以下父兄同伴映画の表示 / rook
rutheniumの化学記号

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2017/02/14 12:05:27」(JST)

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1. シェーグレン・ラルソン症候群 sjogren larsson syndrome

English Journal

Rud syndrome does not exist.

Happle R.
European journal of dermatology : EJD.Eur J Dermatol.2012 Jan-Feb;22(1):7. doi: 10.1684/ejd.2011.1601.
PMID 22067942

Einar Rud and the syndrome that bears his name.

Al Aboud K, Al Aboud D.
European journal of dermatology : EJD.Eur J Dermatol.2011 Nov-Dec;21(6):1025-6. doi: 10.1684/ejd.2011.1547.
PMID 21951511

Rud syndrome with focal cortical dysplasia: a case report.

Marconi S1, Cantalupo G, Marliani F, Toni F, Capovilla G, Lorenzetti E, Romeo A, Michelucci R, Rubboli G.
Brain & development.Brain Dev.2011 Sep;33(8):683-6. doi: 10.1016/j.braindev.2010.10.011. Epub 2010 Nov 12.
We report a female patient with ichthyosis, epilepsy, mental retardation, hypergonadotrophic hypogonadism, polyneuropathy, and cranial dysmorphisms. This clinical picture may satisfy the main diagnostic criteria that characterize Rud syndrome (RS), a rare neurocutaneous disease. The patient underwen
PMID 21074957

Japanese Journal

Rud syndrome with focal cortical dysplasia : A case report

MARCONI Sara,CANTALUPO Gaetano,MARLIANI Federica,TONI Francesco,CAPOVILLA Giuseppe,LORENZETTI Elena,ROMEO Antonino,MICHELUCCI Roberto,RUBBOLI Guido
Brain & development 33(8), 683-686, 2011-09-01
NAID 10031121974

Ｒｕｄ症候群の２例

坪内由里,梅林芳弘,大塚藤男,大久保千眞季,村木良一
西日本皮膚科 56(3), 458-466, 1994
… 11歳の男児と6歳の女児のRud症候群の2例を報告した。 …
NAID 130004473999

Ｒｕｄ症候群

谷崎泰象,中山樹一郎,堀嘉昭,松本忠彦
西日本皮膚科 54(2), 247-250, 1992
… 8歳男子のRud症候群の1例を経験した。 …
NAID 130004473778

Related Links

Rud syndrome | definition of Rud syndrome by Medical dictionary

Rud syn·drome (rūd), ichthyosiform erythroderma associated with acanthosis nigricans, dwarfism, hypogonadism, and epilepsy; mostly sporadic, but may be an X-linked recessive trait. Rud syn·drome (rūd sin'drōm) Ichthyosiform ...