アロポー・ジーメンス症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- German electrical engineer (1816-1892) (同)Ernst Werner von Siemens
- engineer who was a brother of Ernst Werner von Siemens and who moved to England (1823-1883) (同)Karl Wilhelm Siemens, Sir Charles William Siemens
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
UpToDate Contents
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English Journal
- Recessive dystrophic epidermolysis bullosa: presentation of two forms.
- Medenica L1, Lens M.
- Dermatology online journal.Dermatol Online J.2008 Mar 15;14(3):2.
- Dystrophic epidermolysis bullosa (DEB) and aplasia cutis congenita (ACC), also known as congenital localized absence of skin (CLAS) are rare clinical entities. Aplasia cutis congenita presented in conjunction with simplex, junctional, or dystrophic types of epidermolysis bullosa (EB) is classified a
- PMID 18627704
- [Epidermolysis bullosa dystrophica (Hallopeau-Siemens syndrome) of the hand -- surgical strategy and results].
- Diedrichson J1, Talanow D, Safi A.
- Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft für Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft für Mikrochirurgie der Peripheren Nerven und Gefässe : Organ der Vereinigung der Deutschen Plastischen Chirurgen.Handchir Mikrochir Plast Chir.2005 Oct;37(5):316-22.
- Dystrophic epidermolysis bullosa is an inherited, blister-forming skin disease. The Hallopeau-Siemens syndrome type is one of the most severe forms. Even minimal trauma to the skin leads to excessive blister formation that always heals with scars because the defect is located in the dermis at the de
- PMID 16287016
- [Recessive dystrophic epidermolysis bullosa (Hallopeau-Siemens) with IgA nephropathy: 4 cases].
- Farhi D1, Ingen-Housz-Oro S, Ducret F, Rioux-Leclercq N, Cam G, Simon P, Martinez F, Fumeron C, Dubertret L, Blanchet-Bardon C.
- Annales de dermatologie et de vénéréologie.Ann Dermatol Venereol.2004 Nov;131(11):963-7.
- BACKGROUND: The Hallopeau-Siemens type of recessive dystrophic epidermolysis bullosa (HS-RDEB) is a severe hereditary dermatosis, associated with a collagen VII deficiency. A chronic inflammatory syndrome, secondary to recurrent cutaneous infections, may be the cause of AA amyloidosis, with chronic
- PMID 15602383
Related Links
- Hallopeau-Siemens syndrome symptoms, causes, diagnosis, and treatment information for Hallopeau-Siemens syndrome (Dystrophic epidermolysis bullosa) with alternative diagnoses, full-text book chapters, misdiagnosis, research ...
- 1. Handchir Mikrochir Plast Chir. 2005 Oct;37(5):316-22. [Epidermolysis bullosa dystrophica (Hallopeau-Siemens syndrome) of the hand -- surgical strategy and results]. [Article in German] Diedrichson J(1), Talanow D, Safi A. Author ...
★リンクテーブル★
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- 英
- Hallopeau-Siemens syndrome
- 同
- 多発形成障害型表皮水疱症 polydysplastic epidermolysis bullosa
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シーメンス
- 関
- S