WordNet

disorder involving lesions or eruptions of the skin (in which there is usually no inflammation)

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/12/07 21:12:56」(JST)

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1. 自己免疫性甲状腺疾患における前脛骨部粘液水腫（甲状腺皮膚症） pretibial myxedema thyroid dermopathy in autoimmune thyroid disease
2. 爪疾患の概要 overview of nail disorders
3. 進行した腎不全における腎性全身性線維症／腎性線維化性皮膚症 nephrogenic systemic fibrosis nephrogenic fibrosing dermopathy in advanced renal failure
4. 寄生虫妄想症の治療 treatment of delusional parasitosis
5. 甲状腺機能亢進症の診断 diagnosis of hyperthyroidism

Pretibial Myxedema Without Ophthalmopathy: An Initial Presentation of Graves' Disease.

Subramanyam S, Lohiya V, Stahl EJ.SourceDepartment of Internal Medicine (SS, VL), Baptist Health System, Birmingham, Alabama; and Department of Diabetes (EJS), Metabolism & Endocrinology Simon Williamson Clinic, Birmingham, Alabama.
The American journal of the medical sciences.Am J Med Sci.2013 Mar 19. [Epub ahead of print]
OBJECTIVE:: To report a rare case of Graves' disease without ophthalmopathy presenting with pretibial myxedema (PM) as an initial presentation. METHODS:: We present the clinical history, physical findings, laboratory studies and biopsy data of a 62-year-old man with a history of uncontrolled type 2
PMID 23514670

Disruption of lamin B1 and lamin B2 processing and localization by farnesyltransferase inhibitors.

Adam SA, Butin-Israeli V, Cleland MM, Shimi T, Goldman RD.SourceDepartment of Cell and Molecular Biology; Northwestern University Feinberg School of Medicine; Chicago IL USA.
Nucleus (Austin, Tex.).Nucleus.2013 Mar 1;4(2):142-50. doi: 10.4161/nucl.24089. Epub 2013 Mar 1.
Lamin A and the B-type lamins, lamin B1 and lamin B2, are translated as pre-proteins that are modified at a carboxyl terminal CAAX motif by farnesylation, proteolysis and carboxymethylation. Lamin A is further processed by proteolysis to remove the farnesyl, but B-type lamins remain permanently farn
PMID 23475125

Acral milia-like idiopathic calcinosis cutis in a child with down syndrome: report of a case, review of the literature, and description of dermoscopic findings.

Fox GN, Mehregan DA, Jablonowski MN.SourceDefiance Clinic, Defiance, Ohio 43512, USA. foxgary@ yahoo.com
Pediatric dermatology.Pediatr Dermatol.2013 Mar-Apr;30(2):263-4. doi: 10.1111/j.1525-1470.2011.01673.x. Epub 2012 Jan 26.
Milia-like idiopathic calcinosis cutis (MICC) is a rare dermopathy, usually occurring in children with Down syndrome. We report a case of an 8-year-old girl with Down syndrome who presented with histologically verified MICC, briefly review the literature on MICC, discuss the differential diagnosis,
PMID 22276686