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Titolo:
Autosomal dominant burning feet syndrome
Autore:
Stogbauer, F; Young, P; Kuhlenbaumer, G; Kiefer, R; Timmerman, V; Ringelstein, EB; Wang, JF; Schroder, JM; Van Broeckhoven, C; Weis, J;
Indirizzi:
Univ Munster, Dept Neurol, D-48129 Munster, Germany Univ Munster MunsterGermany D-48129 pt Neurol, D-48129 Munster, Germany Univ Aachen, Dept Neuropathol, D-5100 Aachen, Germany Univ Aachen AachenGermany D-5100 pt Neuropathol, D-5100 Aachen, Germany Univ Bern, Inst Pathol, Bern, Switzerland Univ Bern Bern SwitzerlandUniv Bern, Inst Pathol, Bern, Switzerland Univ,Instelling Antwerp, Neurogenet Lab, Flanders Interuniv Inst Biotechnol Univ Instelling Antwerp Antwerp Belgium nders Interuniv Inst Biotechnol
Titolo Testata:
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
fascicolo: 1, volume: 67, anno: 1999,
pagine: 78 - 81
SICI:
0022-3050(199907)67:1<78:ADBFS>2.0.ZU;2-A
Fonte:
ISI
Lingua:
ENG
Soggetto:
MARIE-TOOTH DISEASE; SENSORY NEUROPATHY; LINKAGE; LOCUS; MAPS; 2B;
Keywords:
burning feet syndrome; hereditary sensory neuropathy;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Life Sciences
Citazioni:
19
Recensione:
Indirizzi per estratti:
Indirizzo: Stogbauer, F Univnyunster, Dept Neurol, Albert Schweitzer Str 33, D-48129 Munster, Germa Univ Munster Albert Schweitzer Str 33 Munster Germany D-48129
Citazione:
F. Stogbauer et al., "Autosomal dominant burning feet syndrome", J NE NE PSY, 67(1), 1999, pp. 78-81

Abstract

Familial burning feet syndrome inherited as an autosomal dominant trait has been described in only one family. Due to an associated sensory neuropathy the autosomal dominant burning feet syndrome was suggested to represent avariant form of hereditary sensory and autonomic neuropathy type I (HSAN I). Clinical, histopathological, and molecular genetic studies were performed in a large German kindred with autosomal dominant burning feet syndrome. The autosomal dominant burning feet syndrome was associated with a neuropathy predominantly affecting small unmyelinated nerve fibres. Linkage to the HSAN I locus on chromosome 9q22 and to the Charcot-Marie-Tooth disease type2B (CMT 2B) locus on chromosome 3q13-q22 was excluded. The autosomal dominant burning feet syndrome is neither allelic to HSAN I nor to CMT 2B and thus represents a distinct genetic entity.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 24/01/21 alle ore 15:21:51