Structured Summary
Abstract
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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Classification
Broader headings
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MeSH Record
Synonyms
6 entry terms
- Occult Spina Bifida
- Spinal Bifida, Closed
- Closed Spinal Bifida
- Spina Bifida, Occult
- Dermal Sinus
- Sinus, Dermal
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
1991; was SPINA BIFIDA 1978-1990; for DERMAL SINUS use NEURAL TUBE DEFECTS 1979-1990
MeSH Record
Previous Indexing
- Spinal Dysraphism (1966-1977)
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MeSH Record
NLM Classification
WE 730
AMA Style
References
- National Library of Medicine. Spina Bifida Occulta. Medical Subject Headings (MeSH). 2026. Unique ID D016136. http://id.nlm.nih.gov/mesh/2026/D016136
- Spina Bifida Occulta. In: Wikidata. https://www.wikidata.org/wiki/Q21505502