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Spina Bifida Occulta
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History note: | Spinal Dysraphism (1966-1977)X |
historyNote*: | 1991; was SPINA BIFIDA 1978-1990; for DERMAL SINUS use NEURAL TUBE DEFECTS 1979-1990
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publicMeSHNote*: | 1991; was SPINA BIFIDA 1978-1990; for DERMAL SINUS see NEURAL TUBE DEFECTS 1979-1990
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Scope note: | A common congenital midline defect of fusion of the vertebral arch without protrusion of the spinal cord or meninges. The lesion is also covered by skin. L5 and S1 are the most common vertebrae involved. The condition may be associated with an overlying area of hyperpigmented skin, a dermal sinus, or an abnormal patch of hair. The majority of individuals with this malformation are asymptomatic although there is an increased incidence of tethered cord syndrome and lumbar SPONDYLOSIS. (From Joynt, Clinical Neurology, 1992, Ch55, p34)
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activeMeSHYear*: | |
dateCreated*: | 1990-06-05X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 1999-12-08X |
recordAuthorizer*: | agsX |
recordMaintainer*: | agsX |
recordOriginator*: | AGSX |
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Labels and equivalent concepts: | Selkärangan piilohalkio (fi) XSelkärangan piilotyrä (fi, replaced) Piilevä selkärankahalkio (fi, replaced) Spinal dysrafism (sv, replaced) Spinal Bifida, Closed (en, replaced) Occult Spina Bifida (en, replaced) Spina bifida occulta (la-FI, replaced) |
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