Publication:
Spina bifida: The management of extremity deformities in myelomeningocele

dc.contributor.authorsErol B., Tamai J.
dc.date.accessioned2022-03-15T01:56:11Z
dc.date.accessioned2026-01-10T17:08:46Z
dc.date.available2022-03-15T01:56:11Z
dc.date.issued2008
dc.description.abstractThe spectrum of congenital neural tube defects, referred to as myelomeningocele (spina bifida), produces a wide variety of disabilities, ranging from benign defects in the skin of the back to devastating paralysis and deformity of the lower extremities, urinary and fecal incontinence, hydrocephalus, spasticity, and mental retardation. The care of children with myelomeningocele usually requires a multidisciplinary approach. Early intervention by a team of trained caregivers can significantly improve the disabilities and permit many children to be integrated into normal social environments with high levels of independence. This chapter describes the overall management of myelomeningocele with special emphasis on the orthopedic management. © 2008 Springer-Verlag Italia.
dc.identifier.doi10.1007/978-88-470-0651-5_27
dc.identifier.isbn9788847006508
dc.identifier.urihttps://hdl.handle.net/11424/246841
dc.language.isoeng
dc.publisherSpringer Milan
dc.relation.ispartofThe Spina Bifida: Management and Outcome
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleSpina bifida: The management of extremity deformities in myelomeningocele
dc.typebookPart
dspace.entity.typePublication
oaire.citation.endPage340
oaire.citation.startPage319
oaire.citation.titleThe Spina Bifida: Management and Outcome

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