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. 2011 Oct;6(Suppl 1):S31-40.
doi: 10.4103/1817-1745.85707.

Spinal dysraphism

Affiliations

Spinal dysraphism

N K Venkataramana. J Pediatr Neurosci. 2011 Oct.

Abstract

To review the clinical features and current understanding of spina bifida with an emphasis on the Indian Scenario. Selected articles and current English language texts were reviewed. The authors experience was also reviewed and analysed. Spina bifida is a common congenital anomaly encompassing a wide spectrum of neural tube defects.It is broadly classified as spina bifida aperta and occulta. With the prenatal screening, the incidence of aperta is gradually declining, whereas the detection of occulta has increased with the advent of magnetic resonance imaging. Over the years, the understanding of pathophysiology has made a significant changein the management of these anomalies. Early detection and complete correction can significantly reduce the neurological disability. This article is an overview of spina bifida with a special emphasis on Indian scenario.

Keywords: Aperta; Indian scenario; occulta; spina bifida; tethered cord syndrome.

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Conflict of interest statement

Conflict of Interest: None declared.

Figures

Figure 1
Figure 1
Myelomeningocele
Figure 2
Figure 2
Bifid spine
Figure 3
Figure 3
Bifida spine
Figure 4
Figure 4
Meningocele
Figure 5
Figure 5
Dysplastic skin
Figure 6
Figure 6
Lipoma with tuft of Hair
Figure 7
Figure 7
Tail
Figure 8
Figure 8
Tuft of hair
Figure 9
Figure 9
Dysplastic skin
Figure 10
Figure 10
Imaging of tethering
Figure 11
Figure 11
MRI of tethered cord
Figure 12
Figure 12
Retethering
Figure 13
Figure 13
Lipoma
Figure 14
Figure 14
Terminal lipoma
Figure 15
Figure 15
Lipomyelomeningoceles
Figure 16
Figure 16
Lipomyelomeningocele
Figure 17
Figure 17
Dermal sinus

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