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Titolo:
PURE CONGENITAL FOIX-CHAVANY-MARIE-SYNDROME
Autore:
NISIPEANU P; RIEDER I; BLUMEN S; KORCZYN AD;
Indirizzi:
TEL AVIV UNIV,SACKLER SCH MED,DEPT PHYSIOL & PHARMACOL IL-69978 RAMATAVIV ISRAEL TEL AVIV UNIV,SACKLER SCH MED,DEPT PHYSIOL & PHARMACOL IL-69978 RAMATAVIV ISRAEL
Titolo Testata:
Developmental Medicine and Child Neurology
fascicolo: 10, volume: 39, anno: 1997,
pagine: 696 - 698
SICI:
0012-1622(1997)39:10<696:PCF>2.0.ZU;2-5
Fonte:
ISI
Lingua:
ENG
Soggetto:
OPERCULAR SYNDROME; EPILEPSY; PSEUDOBULBAR; DIAGNOSIS; LESIONS; PALSY;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Science Citation Index Expanded
Citazioni:
17
Recensione:
Indirizzi per estratti:
Citazione:
P. Nisipeanu et al., "PURE CONGENITAL FOIX-CHAVANY-MARIE-SYNDROME", Developmental Medicine and Child Neurology, 39(10), 1997, pp. 696-698

Abstract

Foix-Chavany-Marie syndrome (FCMS) is characterized by facio-linguo-masticatory diplegia in the absence of limb weakness, The most common cause is a cortical lesion resulting from a stroke but a congenital form has been reported, We present the case of a 53-year-old man who was admitted to hospital with worsening dysphagia which was know to have been present together with anarthria and facial palsy, since birth. Xe demonstrated features of FCMS with pseudobulbar palsy and unaffected reflexes and automatic responses. Cranial CT and MRI scans showed bilateral opercular lesions of CSF intensity in continuity with the lateralventricles, We conclude that this case of static FCMS for over 50 years may represent a 'pure' form of congenital FCMS with motor symptomatology and unaccompanied by mental retardation or epilepsy.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 23/09/20 alle ore 22:05:52