Spina bifida

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Spina bifida

Unit 7 Nervous

Unit 7 Nervous

Headaches: Clinical
Headaches: Pathology review
Migraine medications
Migraine
Central nervous system histology
Peripheral nervous system histology
Development of the nervous system
Ascending and descending spinal tracts
Brown-Sequard Syndrome
Syringomyelia
Anatomy of the trigeminal nerve (CN V)
Anatomy of the basal ganglia
Anatomy of the white matter tracts
Anatomy clinical correlates: Vertebral canal
Anatomy of the cerebral cortex
Anatomy of the cerebellum
Basal ganglia: Direct and indirect pathway of movement
Cerebrospinal fluid
Blood brain barrier
Dandy-Walker malformation
Intracerebral hemorrhage
Subdural hematoma
Epidural hematoma
Subarachnoid hemorrhage
Shaken baby syndrome
Normal pressure hydrocephalus
Huntington disease
Movement disorders: Pathology review
Anti-parkinson medications
Parkinson disease
Cluster headache
Tension headache
Chiari malformation
Spina bifida
Cerebral circulation
Cerebellum
Glaucoma
Eye conditions: Refractive errors, lens disorders and glaucoma: Pathology review
Anatomy and physiology of the eye
Anatomy of the eye
Anatomy of the oculomotor (CN III), trochlear (CN IV) and abducens (CN VI) nerves
Eye and ear histology
Anatomy and physiology of the ear
Auditory transduction and pathways
Vestibular transduction
Vertigo: Pathology review
Dizziness and vertigo: Clinical
Otitis media
Pediatric ear, nose, and throat conditions: Clinical
Optic pathways and visual fields
Photoreception
Eye conditions: Retinal disorders: Pathology review
Eye conditions: Inflammation, infections and trauma: Pathology review
Taste and the tongue
Olfactory transduction and pathways
Anatomy of the tongue
Meningitis
Meningitis, encephalitis and brain abscesses: Clinical
Neisseria meningitidis
Mumps virus
Herpes simplex virus
Poliovirus
West Nile virus
West Nile Virus Infection
Trypanosoma cruzi (Chagas disease)
Seizures and epilepsy
Early infantile epileptic encephalopathy (NORD)
Febrile seizure
Seizures: Clinical
Seizures: Pathology review
Nonbenzodiazepine anticonvulsants
Anticonvulsants and anxiolytics: Benzodiazepines
Anticonvulsants and anxiolytics: Barbiturates
Cranial nerves
Cranial nerves rap
Introduction to the cranial nerves
Cranial nerve pathways
Brain tumors: Clinical
Pediatric brain tumors: Pathology review
Adult brain tumors: Pathology review
Knowledge Shot: Glioblastoma
Adult brain tumors
Tuberous sclerosis
von Hippel-Lindau disease
Neurofibromatosis
Anatomy of the limbic system
Schizophrenia
Schizophrenia spectrum disorders: Clinical
Schizophrenia spectrum disorders: Pathology review
Anatomy of the vertebral canal
Anatomy clinical correlates: Spinal cord pathways
Anatomy of the olfactory (CN I) and optic (CN II) nerves
Anatomy of the facial nerve (CN VII)
Anatomy of the glossopharyngeal nerve (CN IX)
Anatomy of the spinal accessory (CN XI) and hypoglossal (CN XII) nerves
Anatomy of the vagus nerve (CN X)
Ischemic stroke
Restless legs syndrome
Acoustic neuroma (schwannoma)
Pediatric brain tumors
Pituitary adenoma
Cauda equina syndrome
Neonatal meningitis
Encephalitis
Bell palsy
Cerebral vascular disease: Pathology review
Spinal cord disorders: Pathology review
Dementia: Pathology review
Anatomy of the inner ear
Emotion
Stroke: Clinical
Broca aphasia
Wernicke aphasia
Delirium
Dementia and delirium: Clinical
Medications for neurodegenerative diseases
General anesthetics
Sleep
Dementia with Lewy bodies
Tricyclic antidepressants
Alzheimer disease
Frontotemporal dementia

Transcript

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With spina bifida, “spina” refers to the spine, while bifida means “split”. So, spina bifida literally means “split spine”. It occurs during embryonal development when the posterior part of the spine doesn’t fully close, leaving behind various degrees of defects, usually in the lumbosacral region of the spine.

To understand spina bifida, we need to zoom in on the embryo during its earliest weeks of development. At this stage, the embryo has three main layers. The ectoderm on the outside, the mesoderm in the middle, and the endoderm on the inside. Around the third week of development, the ectoderm forms a flat sheet of cells known as the neural plate. Soon after, the plate begins to fold inward along the midline, creating a neural groove with raised folds on each side. By the fourth week, these folds move closer and fuse, forming the neural tube. The top part of this tube, called the cranial end, will become the brain, while the bottom part, known as the caudal end, will develop into the spinal cord.

Also, the ectoderm will give rise to three protective layers called the meninges, which wrap around the brain and spinal cord, cushioning them with cerebrospinal fluid. But that’s not all. Thanks to the mesoderm, the body organizes to form structures like muscles, bones, and the overall skeletal framework. This adds another layer of protection because the mesoderm forms the vertebral column that surrounds and protects the spinal cord.

The vertebral column is divided into five regions, each with its own set of vertebrae. The cervical region has 7 vertebrae, labeled C1 to C7; the thoracic region has 12, named T1 to T12; and the lumbar region includes 5, from L1 to L5. Below these, the sacral region consists of 5 fused vertebrae, S1 to S5, and the coccygeal region has 4 fused vertebrae, Co1 to Co4. Now, each vertebra has two main parts. The vertebral body at the front and the vertebral arch at the back. Together, they form a central opening called the vertebral foramen. When the vertebrae stack up, these openings align to create the vertebral canal, which houses the spinal cord.

Now, spina bifida occurs when the caudal end of the neural tube fails to close properly during embryonic development. As a result, the mesoderm above the affected region fails to organize, which results in a defect or absence of the vertebral arches, usually around the L5 to S1 vertebrae.

Depending on the severity of the defect, spina bifida can range from a small, harmless gap in the bone to a complete protrusion of the meninges and the spinal cord through the spine. The exact reason why spina bifida occurs remains a mystery, but several factors can increase the risk. The most important one is not getting enough folic acid during the first trimester of pregnancy because folic acid helps the neural tube close properly. Next, taking certain anti-seizure medications during pregnancy, such as valproic acid, can block folic acid from doing its job, increasing the chance of neural tube defects. Other factors include obesity, consuming alcohol during pregnancy, and poorly controlled diabetes.

Now, depending on the size of the vertebral defect, spina bifida can be classified into several types. First, there’s spina bifida occulta, which is the most common and mildest type. The word occulta means “hidden” because this type often goes unnoticed during prenatal ultrasounds and usually doesn’t cause any symptoms. That’s because, even though one or more vertebrae don’t fully close, the opening is so small that neither the meninges nor the spinal cord can bulge through. Still, subtle signs to keep in mind include a small tuft of hair or a dark patch of skin over the lower back.

Next up is meningocele, which breaks down into “meningo” referring to the meninges, and the suffix “cele” meaning hernia or simply, protrusion. So, in this type, the meninges slip through a gap in the vertebrae and form a visible sac on the lower back, filled with cerebrospinal fluid. Since the spinal cord itself stays in place within the spinal canal, the risk of neurologic complications is usually low.

Key Takeaways

Spina bifida is a congenital birth defect of embryonic development where there is incomplete closing of the vertebral column and membranes around the spinal cord. There are three main types: spina bifida occulta, meningocele, and myelomeningocele. In Spina bifida occulta there is only a small gap in the bones of the spine, and the spinal cord and surrounding tissue don't protrude. In meningocele, the meninges protrude through the opening in the spinal column, but the spinal cord itself is not affected. In myelomeningocele, there is a protrusion of the spinal cord and nerves through the opening of the spinal cord. For treatment, prenatal surgery is done to close myelomeningocele, but this surgery can be dangerous to the developing fetus as well as the mother. In cases where postnatal surgery is chosen, it is often done within the first few days of an infant's life to minimize the risk of infection like meningitis.

Sources

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