2. Neural groove- dorsum of embryo
Deepens- Furrow
Closes- Neural canal
CENTRAL NERVOUS SYSTEM
4th
week of IUL
3. Lumen persists as – Central neural canal.
Closure
◦ Starts in cervical region
◦ Proceeds caudally & cranially
◦ Cranium closing last – 26 days
Neural tube
◦ Proliferating cells of neuroepithelium differentiate –
NEUROBLASTS or NEURONS.
Motor axons – out growing processes.
Sensory neurons – from neural crests (Ectoderm & Post
surface of neural tube).
4. Meninges – arise from loose mesenchymal
tissue surrounding the N. tube.
◦ Pia mater – 40 days
◦ Dura – later.
Neural canal separates from ectodermal
covering – ingrowth of mesoderm.
Notochord –
◦ solid rod of cells
◦ Anterior to N. canal
Vertebral bodies develop around this all.
5. From each of the Vertebral bodies
◦ Extend backwards 2 projections
◦ Grow around N. canal
◦ Form – Vertebral arch
◦ Fuse behind thoracic region – extend up & down.
6. FUSION FAILS – Gap in vertebral N arch
SPINA BIFIDA
◦ m.c. in Lumbosacral region
7. Latin word for “split spine”.
Literally means “cleft spine,”
Most common group of birth defects called neural
tube defects (NTD).
Incidence
◦ World wide about 1 per 1000 live births.
8. Antenatal screening of AFP - 15–18 mths.
◦ Identify at risk women.
◦ If high AFP – Amniocentesis and USG.
Previous neural tube defect fetus –
◦ 10 fold increased risk
◦ 50 fold for third pregnancy.
Genetic predisposition.
Some environmental factors
9. The exact cause of spina bifida remains a
mystery.
Genetic, nutritional, and environmental
factors may play a role.
Combination of genetic and environmental risk
factors, such as a family history of neural tube
defects, folic acid deficiency and medical
conditions such as diabetes and obesity.
10. Race: more common among Hispanics and
whites of European descent.
Family history of neural tube defects.
However, most babies with spina bifida are born
to parents with no known family history of the
condition.
11. Folic acid deficiency (vitamin B-9)
increases the risk of spina bifida and other
neural tube defects.
◦ MRC recommend F. acid supplimentation for high risk
mothers.
Some medications. Anti-seizure medications,
such as valproic acid, seem to cause neural
tube defects when taken during pregnancy,
perhaps because they interfere with the body's
ability to use folic acid.
12. Diabetes: Especially when the mother's blood
sugar is elevated early in her pregnancy. Much
of this risk is preventable by careful blood sugar
control and management.
Obesity. There's a link between pre-pregnancy
obesity and neural tube birth defects, including
spina bifida. Obese women may have more
babies with spina bifida possibly because of
nutritional deficits from poor eating habits or
because they may have diabetes.
13. Increased body temperature. Some evidence
suggests that increased body temperature
(hyperthermia) in the early months of pregnancy
may increase the risk of spina bifida.
Contaminated potatoes – blamed in humans.
Experimental defects – Vit A def., Azodyes, X rays
& disturbed Zn metabolism.
14. Von Recklinghausen 1886
◦ Due to failure of the posterior mass of neural tube.
16. Saccular trusion of
only meninges
Pia &
Arachnoid
Dura stops at bony
margins
Spinal cord is not involved
No paralysis
Sac contains only CSF
17. 5 % of Spina bifida cystica.
Surgical closure required – to prevent rupture and
meningitis.
Associated lesions
◦ Lipomata
◦ Cyst formation
◦ Dilation of spinal canal – hydromyelin.
18. Majority of SBC
Gap in spinal column
through which protrudes
1. Flat plaque of N. tissue.
2. Meninges surrounding it.
Spinal cord – open on the
back surface for 3-4
segments.
19. Plaque and meninges – enlarge to sac –
increasing CSF within few hours of birth.
Sac – burst – during or just after birth.
CSF leak – infection.
3 Zones on surface:
1. Central neural plaque (Vasculosa)
2. The meninges (Serosa)
3. Surrounding hairy & thickened skin (Dermatica)
20. Spinal cord is spread out to form lining of the sac
& is thinned into a cyst by distension of central
canal of the cord.
21. Myelocele:
◦ Gross spinal cord deformity
◦ Elongated fissure surrounded by telangiectases or hair –
in direct contact with central canal.
◦ m.c. in lumbosacral region.
Anterior Spina Bifida
◦ Very rare – anterior defect.
22. Often unnoticed
Incidentally on radiograph.
Spinal cord and meninges normal
One or more bony arches are incompletely closed
posteriorly.
Dura may be attached to skin – fibrous band –
MEMBRANA REUNIENS
23. Lipomata or Angiomata – in or outside the
vertebral canal.
Hairy patch – overlying skin.
Membrana reuniens doesn’t elongate with growth
– traction lesion of cord – praralytic deformity of L
limbs or bladder.
24. Called by Till - Occult spinal dysraphism:
1. Diplomyelia
2. Diastematomyelia
3. Others – Intraspinal lipomata or hydromyelia of central
canal.
Urinary incontinence, neurological abnormalities
(esp in L limbs) or meningitis by infected dermal
sinus.
Need Radiography, myelography or MRI before
surgery.
25. The American Academy of Orthopaedic
Surgeons Committee for the Care of the
Handicapped Child (1974)
1. Open defects:
1. Myelomeningocele (Hydromyelia, dysraphism
rachischisis)
2. Meningocele
3. Dermal sinus.
27. 3. Errors in skeletal segmentation:
1. Absence of sacrum
2. Absent lumbar vertebrae
3. Hemivertebrae
4. Congenital segmental fusion
5. Failure of fusion or absent odontoid process
6. Others.
28. Stark & Baker (1967) – two main types:
◦ TYPE-I (~33%) – Complete loss of all spinal cord funtion
below the lesion level – flaccid paralysis, sensory
deficiency & absent reflexes.
◦ TYPE-II (~66%) – Preservation of reflex activities from
intact distal segment but interruption corticospinal tracts
with paralysis. Three subgroups depending on severity.
29. Early operation at 48 hrs. without selection – Initial
optimism – by Sharrard
◦ Survival rate improved
◦ Quality of life – pitiful.
30. Lorber 1971 defined factors associated with bad
prognosis – used as basis for selection:
◦ Gross paralysis in TLS region.
◦ Esp with scoliosis or kyphosis
◦ Enlarging hydrocephalus
◦ Intracerebral injury
◦ Heart abnormality
◦ Meningitis or gross mental disturbance.
31. Principles of combined management – by
Sharrard et. al in Sheffield – directed to 5 major
problems:
1. Myelomeningocele
2. Hydrocephalus
3. Urinary tract paralysis
4. Locomotor system
5. Education
32. To achieve INDEPENDENCE as
far as possible.
Role of Orthopaedic surgeon –
provide – by surgical or non
surgical means, the ability to sit
and stand as well as effective but
not excessive demanding
walking.
33. Surgical closure of myelomeningocele – whenever
indicated – within 48hrs.
Baseline neurological examination, head
circumference & assessment of any hip
dislocation.
Hydrocephalus drained from dilated lateral
ventricle.
