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[Arthrogryposis multiplex congenita]. / Arthrogryposis multiplex congenita
Linnet, Karen Markussen; Balslev, Thomas; Møller-Madsen, Bjarne.
Afiliação
  • Linnet KM; Børneafdelingen, Aarhus Universitetshospital, Palle Juul-Jensens Boulevard 99, 8200 Aarhus N. karelinn@rm.dk.
Ugeskr Laeger ; 177(33): V12140712, 2015 Aug 10.
Article em Da | MEDLINE | ID: mdl-26320355
ABSTRACT
Arthrogryposis multiplex congenita (AMC) is a sign rather than a diagnosis. It implies contractures in multiple body areas and occurs in 13,000-5,000 live births. Primary aetiologies include neuropathic, myopathic, metabolic, end plate and vascular disorder affecting the developing foetus, including limitation of foetal space. Amyoplasia is the most common type of AMC after central nervous system disorders. Knowledge about the classification of AMC is essential to make a correct diagnosis and treatment plans. We recommend follow-up by experienced paediatric orthopaedic surgeons and neurologists.
Assuntos
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Bases de dados: MEDLINE Assunto principal: Artrogripose Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Humans / Infant Idioma: Da Revista: Ugeskr Laeger Ano de publicação: 2015 Tipo de documento: Article
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Bases de dados: MEDLINE Assunto principal: Artrogripose Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Humans / Infant Idioma: Da Revista: Ugeskr Laeger Ano de publicação: 2015 Tipo de documento: Article