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Radicular dysfunction due to spinal deformities in Marfan syndrome at older age: three case reports.
Voermans, N C; Hosman, A J; van Alfen, N; Bartels, R H; de Kleuver, M; op den Akker, J W; van Engelen, B G.
Afiliação
  • Voermans NC; Donders Centre for Neuroscience, Department of Neurology, Radboud University Nijmegen Medical Centre, The Netherlands. n.voermans@neuro.umcn.nl
Eur J Med Genet ; 53(1): 35-9, 2010.
Article em En | MEDLINE | ID: mdl-19879983
ABSTRACT
Marfan syndrome is a inherited connective tissue disorder due to mutations in fibrillin-1. It presents with cardiovascular, ocular, skeletal, pulmonary and dural signs and symptoms. Some of the symptoms of later onset are those associated with scoliosis and dural ectasia. This is the enlargement of the neural canal especially in the lower lumbar and sacral region and occurs in over 90% of Marfan patients. We here report three patients with lumbar and/or sacral radiculopathy due to (kypho)scoliosis and dural ectasia with spinal meningeal cysts. The pain, muscle weakness, muscle atrophy, and sensory disturbances illustrate the severe neurological complications which may occur in Marfan syndrome, especially at later age. Awareness of these complications and development of management protocols is essential since life expectancy of Marfan patients has increased. Marfan syndrome might gradually become recognized as an inherited connective tissue disorder with potentially severe neurological complications during ageing.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Região Sacrococcígea / Envelhecimento / Vértebras Lombares / Síndrome de Marfan Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Med Genet Ano de publicação: 2010 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Região Sacrococcígea / Envelhecimento / Vértebras Lombares / Síndrome de Marfan Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Med Genet Ano de publicação: 2010 Tipo de documento: Article