Dandy-Walker malformation

Last updated: February 24, 2023

Dandy-Walker malformation

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
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Anatomy of the olfactory (CN I) and optic (CN II) nerves
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Transcript

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Dandy-Walker malformation, first described by Dr. Walter Dandy and Dr. Arthur Walker, is a congenital brain defect where there’s a cystic malformation in the cerebellum that blocks cerebrospinal fluid from exiting the brain.

This results in increased intracranial pressure and can affect the cerebellum’s ability to control motor skills like walking.

The cerebellum, or "little brain", sits just below the main part of the brain and it’s divided at the midline into two hemispheres by a short worm-like structure called the vermis.

The cerebellum is contained within the back of the skull, in an area known as the posterior fossa, and it sits above the foramen magnum, an opening at the base of the skull through which the spinal cord enters.

The cerebellum controls balance and posture, and helps to initiate as well as fine-tune voluntary motor activity - think about the fancy finger work of a piano player or the vocal cords of a singer - that’s the cerebellum in action.

Now, within the brain there are also four interconnected cavities called ventricles, each of which create and help circulate cerebrospinal fluid.

Highest up, are two C-shaped lateral ventricles that lie deep in each cerebral hemisphere.

The two lateral ventricles drain their cerebrospinal fluid into the third ventricle, which is a narrow, funnel-shaped, cavity at the center of the brain.

The third ventricle makes a bit more cerebrospinal fluid and then sends all of the cerebrospinal fluid to the fourth ventricle via the cerebral aqueduct.

The fourth ventricle is a tent-shaped cavity located between the brainstem and the cerebellum and is continuous with the central canal.

After the fourth ventricle, the cerebrospinal fluid enters the subarachnoid space, which is the space between the two inner linings of the brain - the arachnoid and pia mater.

In a Dandy-Walker malformation, there are three main defects.

First, there’s a cyst in the fourth ventricle which causes the ventricle to enlarge and as a result it presses against the cerebellum, interfering with cerebellar function.

Key Takeaways

Dandy-Walker malformation (DWM) is a congenital brain defect in which the 4th ventricle fails to close. It is characterized with a cysts in the 4th ventricle, hypoplasia of the cerebellar vermis, and enlargement of the posterior cranial fossa. This condition results in hydrocephalus, increased intracranial pressure, and a characteristic "dandy walker" appearance on neuroimaging.

Symptoms of DWM vary depending on the degree of cerebellar hypoplasia. Patients may experience delayed milestones, hypotonia, ataxia, vomiting, and seizures. Hydrocephalus can cause enlargement of the head (macrocephaly) and bulging fontanelles.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
  4. "CURRENT Medical Diagnosis and Treatment 2020" McGraw Hill Professional (2019)
  5. "The Most Common Comorbidities in Dandy-Walker Syndrome Patients: A Systematic Review of Case Reports" Journal of Child Neurology (2017)
  6. "Hydrocephalus in Dandy–Walker malformation" Child's Nervous System (2011)
  7. "Dandy-Walker malformation: prenatal diagnosis and prognosis" Child's Nervous System (2003)