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Titolo:
Fibrodysplasia ossificans progressiva: Report of two cases
Autore:
Fonseca, JE; Branco, JC; Reis, J; Evangelista, T; Tavares, V; Gomes, AR; Queiroz, MV;
Indirizzi:
Egas Moniz Hosp, Rheumatol Unit, Lisbon, Portugal Egas Moniz Hosp LisbonPortugal Hosp, Rheumatol Unit, Lisbon, Portugal Hosp Santa Maria, Dept Orthopaed, Lisbon, Portugal Hosp Santa Maria Lisbon Portugal aria, Dept Orthopaed, Lisbon, Portugal Hosp Santa Maria, Dept Neurol, Lisbon, Portugal Hosp Santa Maria Lisbon Portugal a Maria, Dept Neurol, Lisbon, Portugal Garcia da Orta Hosp, Rheumatol Unit, Almada, Portugal Garcia da Orta HospAlmada Portugal p, Rheumatol Unit, Almada, Portugal Hosp Santa Maria, Unidade Reumatol, P-1600 Lisbon, Portugal Hosp Santa Maria Lisbon Portugal P-1600 eumatol, P-1600 Lisbon, Portugal
Titolo Testata:
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
fascicolo: 6, volume: 18, anno: 2000,
pagine: 749 - 752
SICI:
0392-856X(200011/12)18:6<749:FOPROT>2.0.ZU;2-N
Fonte:
ISI
Lingua:
ENG
Soggetto:
BONE MORPHOGENETIC PROTEIN-4;
Keywords:
ectopic ossification; etidronate; fibrodysplasia ossificans progressiva; surgery;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Life Sciences
Citazioni:
31
Recensione:
Indirizzi per estratti:
Indirizzo: Fonseca, JE Hosp Santa Maria, Unidade Reumatol, Av Prof Egas Moniz, P-1600Lisbon, Portugal Hosp Santa Maria Av Prof Egas Moniz Lisbon Portugal P-1600 al
Citazione:
J.E. Fonseca et al., "Fibrodysplasia ossificans progressiva: Report of two cases", CLIN EXP RH, 18(6), 2000, pp. 749-752

Abstract

Fibrodysplasia Ossificans Progressiva (FOP) is a rare hereditary connective tissue disease, genetically inherited as an autosomal dominant tr ait with complete penetrance but variable expressivity. Onset is typically in childhood and progressive involvement of the spine and proximal extremities leads to immobility and articular dysfunction. We present two cases with the typical features of FOP and a review of the pathogenesis, clinical manifestations and treatment options of this rare disease.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 04/12/20 alle ore 00:39:31