CareLit · DOI-Nachweis · Klinische Neurophysiologie
Isolated paraspinal myopathy: a distinct subtype of facioscapulohumeral muscular dystrophy
DOI 10.1055/s-2006-939150
Bibliografische Angaben
Nachweis in CareLit
Autor:innenF Glocker, G Meng, M Kottlors
ZeitschriftKlinische Neurophysiologie
Ausgabe03/2006
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Fascioscapulhumeral muscular dystrophy (FSHD) is inherited as an autosomal dominant trait and is characterized by facial and shoulder girdle weakness usually appearing in adolescence. In milder cases signs may be apparent not before late adulthood. A scapuloperoneal subtype sparing the facial muscles has been described. We present two cases with genetically confirmed FSHD with a distinct phenotype solely affecting t…
Zitieren
Zitierempfehlung
F Glocker, G Meng, M Kottlors (2006) Isolated paraspinal myopathy: a distinct subtype of facioscapulohumeral muscular dystrophy. Klinische Neurophysiologie (03). https://doi.org/10.1055/s-2006-939150
Mit CareLit weiterarbeiten