24.3 Movement disorders Flashcards
Define athetosis, dystonia, tics, chorea, tremor, restless leg syndrome and ataxia.
What is cerebral palsy?
An umbrella term for non-progressive neurological and physical disabilities caused by damage or a lesion to a child’s brain early in life or in utero.
It is the most common congenital cause of physical impairment.
What is the range of disability with regards to cerebral palsy?
- Monoplegia: affects 1 limb
- Paraplegia: affects 2 limbs
- Quadriplegia: affects 4 limbs
- Hemiplegia: affects limbs on one side
How is brain damage caused in cerebral palsy?
Mainly due to hypoxia, trauma or infection.
E.g. a long and difficult birth.
What are the risk factors for cerebral palsy?
- Maternal age lower than 20 or above 35
- Pre-eclampsia
- Prenatal irradiation
- Pre-natal infections e.g. rubella, syphilis, cytomegalovirus
- Peri-natal risks (during birth) e.g. traumatic or breach birth, prolonged delivery
- Post-natal infections e.g. meningitis, encephalitis
What are the 5 types of cerebral palsy?
- Spastic CP (most common, 77%)
- Athetoid cerebral palsy
- Ataxic CP
- Hypotonic CP
- Mixed type
What are the features of cerebral palsy?
- Visual, hearing and speech impairments
- May have a learning disability
- Weakness in one or more limbs, foot that drags as they walk
- Non-progressive
- Secondary complications can occur
- Epilepsy may also be present
- Dysphagia
- Excessive drooling
- Poor control over hand and arm movements
- Abnormal gait
What secondary complications might someone with cerebral palsy experience?
- Respiratory complications due to dysphagia
- Gastric reflux
- Constipation due to reduced muscle tone
- Bladder and kidney infections
- Pressure sores on the skin
- Peri-oral skin issues due to drooling
- Musculo-skeletal issues e.g. arthritis, dislocations, deformities
What dental considerations are there with regards to people with cerebral palsy?
- Developmental abnormalities: maxillary arch often tapered, labially inclined incisors, malocclusion may be more common due to poor oromuscular co-ordination, lack of lip seal and tongue thrust
- Uncontrolled movement: spacicity of TMJ musuclature, spontaneous jaw dislocation, spontaneous subluxation of TMJ, facial grimacing
- Bruxism and tooth wear due to uncontrolled movement of TMJ muscles, may be exacerbated by reflux
- Periodontal disease: mouth breathing, anti-epileptic medication can cause gingival enlargement, increased food retention, poor mobility so poor OH, if they are PEG fed they will have lots of calculus
- Caries: food retention, struggle with OH, dietary supplements may be cariogenic
- Truama: increased risk of falls and seizures
- Xerostomia: reduced salivary flow rate and lower buffering capacity, medication may also cause xerosotmia
- Sialorrhea: excessive drooling
How can sialorrhea be managed?
- Anticholinergic drugs e.g. glycopyrronium bromide
- Botox can be used, effects last 2-6 months
How may cerebral palsy affect dental treatment?
- Setting depends on severity, some pts can be treated in primary care
- Consider ability to consent, CP doesn’t mean someone doesn’t have the intellect to consent always
- Sedation may be required, jerky movements can affect treatment
- Support pts head with pillow
- GA may be needed
- Hoist in hospitals or specialist dental practice to get pt into chair
What is Huntington’s disease?
A hereditary neurodegenerative disorder.
- Huntington gene on chromosome 4
- Autosomal dominant
- Causes damage to the basal ganglia and cerebral cortex
- Symptoms develop aged 30-50
What are the signs and symptoms of Huntington’s?
- Early symptoms include uncontrollable muscle movements, clumsiness, stumbling when walking, lack of concentration, mood and personality changes, depression, aggression, problems remembering new facts, difficulty making decisions and driving
- As disease progresses, speech becomes slurred, swallowing and eating difficulties arise, walking becomes difficult and patient may require a wheelchair
- Cognitive decline can result in dementia
- Duration of disease is 10-30 years after diagnosis
- Triad of symptoms: movement, cognition, mental health
What is the management for Huntington’s?
- No specific treatment
- Medicines can help to improve quality of life
- Antipsychotic/neuroleptic medicines help muscle movement and mood changes
- Antidepressants can stabilise the mood e.g. fluoxetine, sertraline, citalopram, quetiapine, olanzapine, risperidone
- Speech and language therapy to help speech and swallowing issues
What are the dental considerations with regards to patient’s with Huntington’s?
- Oral hygiene affected by poor manual dexterity and cognitive decline
- As condition progresses, capacity to consent may be lost
- Communication difficulties, struggle to understand complex sentences
- Mobility, will eventually require a wheelchair
- PEG feeding = calculus
- Trauma to soft tissues
- Medications can cause xerostomia, xerostomia can lead to candida
- Open mouth posture can exacerbate xerostomia
- Vomiting and reflux can damage dentition and cause ulcers