Developmental Disorders Part 2 Flashcards

1
Q

Intellectual disabilities are?

A

Type of developmental disability that must occur before the age of 18 and be characterized by significant subaverage general intellectual function and limitations in adaptive functioning

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2
Q

What percentage of the general population have intellectual disabilities?

A

2.5-3%

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3
Q

When do intellectual disabilities begin?

A

18 years or younger

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4
Q

What is the IQ score range for someone with an intellectual disability?

A

70-75

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5
Q

What are the severities of ID?

A

Mild, moderate, severe, profound

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6
Q

What percentage of individuals with ID have mild ID?

A

80%

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7
Q

What is the IQ level of someone with mild ID?

A

50-75

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8
Q

What percentage of individuals with ID have moderate ID?

A

10%

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9
Q

What is the IQ level of someone with moderate ID?

A

35-55

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10
Q

What percentage of individuals with ID have severe ID?

A

3-4%

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11
Q

What is the IQ level of someone with severe ID?

A

20-40

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12
Q

What percentage of individuals with ID have profound ID?

A

1-2%

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13
Q

What is the IQ level of someone with profound ID?

A

20-25

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14
Q

Etiology of ID

A

Genetic Conditions:
Down syndrome, Fragile X syndrome, and other chromosomal abnormalities
Prenatal Factors:
Maternal infections, substance abuse during pregnancy, and exposure to
toxins
Perinatal Factors:
Complications during labor and delivery, such as oxygen deprivation
Postnatal Factors:
Infections, head injuries, or severe malnutrition during early childhood

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15
Q

Oral manifestations observed in patients
with ID

A
  • Self-biting
  • Bruxism
  • Thick, flaccid lips
  • Microdontia
  • Malocclusion
  • Delayed tooth eruption
  • Dental attrition and sensitivity
  • TMJ disorder
  • Periodontal Disease
  • Heavy plaque accumulation
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16
Q

Health-related characteristics of ID

A
  • Less physical stamina
  • Delayed physical development
  • Speech
  • Poor motor control
  • Poor vision
  • Poor hearing
  • Overweight/underweight
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17
Q

Mental and motor ability characteristics of ID

A
  • Short memories
  • Inability to concentrate or see differences
    or likeness
  • Limited speech
  • Lack of organized skills
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18
Q

Social and emotional ability characteristics of ID

A
  • Imitate others
  • Aggressiveness towards others
  • Property destruction
  • Self injury
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19
Q

Self-injurious behavior (SIB) characteristics of ID

A
  • Head-banging
  • Self-biting
  • Bruxism
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20
Q

Visual, hearing, and speech disabilities occurring in those ages 15 + statistics

A
  • 6 mil sight difficulties
  • 6.8 mil hearing difficulties
  • 2.1 mil speech difficulties
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21
Q

Visual disabilities can range from?

A

partial sight to total blindness

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22
Q

Common causes of visual disabilities include?

A
  • cataracts
  • glaucoma
  • macular degeneration
  • diabetic retinopathy
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23
Q

How many people worldwide have vision problems?

A

285 mil

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24
Q

What are treatments for visual impairments?

A
  • Corrective lenses (glasses or contacts)
  • Surgery (cataract surgery or corneal
    transplants)
  • Low vision aids (assistive technology)
  • Orientation and mobility training
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25
Q

Hearing disabilities can vary from?

A

mild hearing loss to profound deafness

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26
Q

Causes of hearing impairment include

A

age-related hearing loss, exposure to loud
noises, infections, and genetic factors

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27
Q

How many people worldwide experience hearing loss?

A

Over 466 million

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28
Q

Treatment for hearing loss includes?

A
  • Hearing aids
  • Cochlear implants
  • Speech therapy
  • Sign language
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29
Q

Speech disabilities include?

A
  • Difficulties with articulation, fluency, or
    voice quality
  • Conditions like stuttering, dysarthria, and
    aphasia
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30
Q

When are speech disabilities often identified?

A

Early childhood

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31
Q

Treatment for speech disabilities include?

A
  • Speech therapy
  • Augmentative and alternative
    communications (comm. boards or apps)
  • Behavioral therapy
  • Medical intervention (Botulinum toxin
    injections are used to treat spasmodic
    dysphonia (voice box spasms) by
    temporarily paralyzing the
    affected muscles)
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32
Q

Learning disabilities

A

neurological disorders that
affect the brain’s ability to receive,
process, store, and respond to
information

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33
Q

Many people with LD have above average intelligence, true or false?

A

True

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34
Q

What percentage of the population is affected by LD?

A

5-15%

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35
Q

Psychiatric disorders

A

mental health disorders, encompass
a wide range of conditions that affect mood, thinking, and behavior

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36
Q

Statistically how many people are affected by mental illness annually?

A

1 in 5 adults

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37
Q

Symptoms of a psychiatric disorder may include?

A
  • Changes in mood (e.g., persistent sadness
    or irritability)
  • Altered thinking (e.g., paranoia or
    distorted reality)
  • Changes in behavior (e.g., withdrawal or
    changes in sleep and appetite)
  • Difficulty concentrating or making
    decisions
  • Increased anxiety or fear responses
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38
Q

Treatment of psychiatric disorders include?

A
  • Psychotherapy (cognitive behavior therapy, dialect behavior therapy, exposure therapy)
  • Medications (antidepressants, antipsychotics, mood stabilizers)
  • Support groups
  • Psychoeducation
  • Crisis support
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39
Q

Cognitive Behavioral Therapy (CBT)

A

Focuses on changing negative thought patterns and behaviors

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40
Q

Dialectical Behavior Therapy (DBT)

A

Often used for borderline personality disorder; combines cognitive-behavioral techniques with mindfulness

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41
Q

Exposure Therapy

A

Particularly effective for anxiety disorders and PTSD

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42
Q

Spinal Bifida

A

Congenital condition that occurs when
the spinal column doesn’t close completely around the spinal cord during early fetal development

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43
Q

Most common
permanently disabling
birth defect in the U.S. is?

A

Spinal Bifida

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44
Q

Spina Bifida Occulta

A

The mildest form, where there’s a small defect in the spine that often goes unnoticed. It may cause no symptoms or only minor issues (15-20% of people)

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45
Q

Meningocele

A

Involves a sac of fluid that protrudes through the opening in the spine, but
the spinal cord remains in place. This may require surgery

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46
Q

Myelomeningocele

A

The most severe form,
where both the spinal cord and nerves protrude through the opening. Causes neurological impairment and requires surgical intervention

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47
Q

Symptoms of spinal bifida are?

A
  • Physical disabilities (varying
    levels of mobility)
  • Bladder and bowel issues
  • Learning difficulties
  • Hydrocephalus (accumulation
    of fluid in the brain)
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48
Q

Etiology of spinal bifida

A
  • Genetic factors
  • Nutritional deficiencies
  • Maternal health
  • Environmental factors
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49
Q

Genetic factors in spinal bifida

A

A family history of neural tube
defects

50
Q

Nutritional deficiencies in spinal bifida

A

Lack of folic acid during pregnancy

51
Q

Maternal health factors in spinal bifida

A
  • Conditions like diabetes or
    obesity can increase risk
  • High temperatures in early pregnancy (i.e.,
    prolonged fevers and hot tub use)
52
Q

Environmental factors in spinal bifida

A
  • Certain medications
    (antipsychotics) and exposure to harmful
    substances
  • Previous NTD (neural tube defect) -
    affected pregnancy increases a woman’ s
    chance to have another NTD-affected
    pregnancy by approximately 20 times
53
Q

Treatment for spinal bifida

A
  • Surgery
  • Rehabilitation
  • Supportive care
54
Q

Fetal alcohol syndrome

A

Condition resulting from alcohol exposure during pregnancy. It is part of a spectrum of disorders known as Fetal Alcohol Spectrum Disorders (FASDs), which can lead to a range of physical, behavioral, and cognitive issues in the affected child

55
Q

How many infants are affected by FAS each year?

56
Q

What is the 3rd most common intellectual disability worldwide

57
Q

Seen on every part of the body, including brain, face, eyes, ears, heart, kidneys, and bones

58
Q

FAS symptoms

A
  • Distinctive facial features, including small
    eyes, an exceptionally thin upper lip, a
    short, upturned nose, and a smooth skin
    surface between the nose and upper lip
  • Heart defects
  • Deformities of joints, limbs, and fingers
  • Slow physical growth before and after
    birth
  • Vision difficulties or hearing problems
  • Small head circumference and brain size
  • Poor coordination
  • Sleep problems
  • Intellectual disability and delayed
    development
  • Learning disorders
  • Abnormal behavior, such as a short
    attention span, hyperactivity, poor
    impulse control, extreme nervousness,
    and anxiety
59
Q

Epilepsy

A

Seizure disorder in which the excessive abnormal neuronal discharges from cerebral functions disturbances are recurrent. The specific underlying brain dysfunction causing the seizure disorder can be identified only in approx. half of childhood-onset and adult-onset seizures

60
Q

Statistics of those who have epilepsy

A

3.4 million people in the U.S., and over 65 million people worldwide

61
Q

Tonic-Clonic Seizures (grand-mal)

A

Most common
- Several Phases:
- Aura: occurs hours to days before seizure
- Tonic: body stiffness
- Clonic: Convulsions
- Loss of bladder

62
Q

Absence (Petit Mal) Seizures

A

Familial
- Occur exclusively in childhood (3-12yrs)
- Seizure consists of brief (10-30 seconds)
altered states
of consciousness
- Vacant stare/Eyelid blinking/ Lip smacking
- Child has no recollection of seizure and
goes back to normal

63
Q

Status Epilepticus

A
  • Defined as a single seizure lasting for at least 30 minutes OR recurrent generalized seizures without regaining of consciousness between the seizure episodes
    *** Life- threatening medical emergency that can lead to irreversible neurologic damage and requires prompt intensive therapy
64
Q

Seizure causes

A
  • Genetic: Inborn errors of metabolism
  • Congenital abnormalities: Maldevelopment of brain
  • Perinatal: Anoxia, ischemia, hemorrhage
  • Central nervous system infections: Encephalitis, meningitis, abscess
    Trauma: Penetrating wound, closed-head injury, surgery
  • Neoplastic: Primary gliomas, metastatic
  • Vascular: Infarction, hemorrhage, arteriovenous malformations
  • Toxic: Alcohol or cocaine use, alcohol and sedative drug withdrawal
  • Metabolic: Hypoglycemia, hypocalcemia, high fever
  • Degenerative: Alzheimer disease, Creutzfeldt- Jakob disease
65
Q

What classification of ASA is someone who has seizures?

66
Q

NO2 should not be used in patients who experience what?

A

Seizures, it can invoke them

67
Q

Alzheimer’s disease

A

Brain degenerative disorder that gradually destroys the ability to remember,
reason, learn and imagine

68
Q

What is the most common type of dementia?

69
Q

What is the 6th leading cause of death in the US?

70
Q

How long from the first onset of symptoms of AD does someone usually have to live?

71
Q

What are some medication treatments to slow the progression of AD?

A

Acetylcholine drugs are used to improve cognition. Their effects are not permanent

72
Q

CVA/stroke

A

occurs when blood flow to a
part of the brain is interrupted or
reduced, depriving brain tissue of
oxygen and nutrients. When brain cells
are deprived of oxygen, they begin to die
within minutes, potentially leading to
long-term neurological impairments or
death if not treated swiftly

73
Q

What is the major cause of serious, long-
term disabilities in adults

74
Q

Ischemic Stroke

A

This is the most
common type, accounting for about
87% of all strokes. It occurs when a
blood clot blocks or narrows an
artery leading to the brain, often
due to atherosclerosis (buildup of
plaque in the arteries)

75
Q

Hemorrhagic Stroke

A

This type results from hemorrhage or rupture of a brain vessel, which causes
leakage of blood into the brain
tissue, the ventricles, or the space
between the brain and skull

76
Q

Transient Ischemic Attack
(TIA)

A

Often called a “mini-stroke,” a
TIA occurs when blood flow to the
brain is briefly interrupted. While
symptoms may resolve within
minutes, a TIA is a serious warning
sign of a potential future stroke.
Followed by a complete clinical
recovery

77
Q

Symptoms of a stroke

A
  • Weakness or numbness, often on one
    side of the body (face, arm, or leg)
  • Difficulty speaking or understanding
    speech
  • Vision problems in one or both eyes
  • Severe headache, sometimes
    accompanied by vomiting or dizziness
  • Difficulty with balance or coordination
78
Q

What does FAST stand for?

A

Face drooping
Arm weakness
Speech difficulties
Time to call

79
Q

The side of the face and body affected by stroke is opposite that of the brain injury, true or false?

A

True, because the sensory and motor neurons cross as they go to/from the cerebral cortex

80
Q

RIGHT SIDE BRAIN DAMAGE

A
  • Paralyzed left side
  • Spatial or perceptual deficits
  • Impaired thought process
  • Quick, impulsive behavior
  • Patient cannot use a mirror
  • Difficulty preforming tasks: ex. Toothbrushing
  • Memory deficits
  • Neglect of left side
81
Q

LEFT SIDE BRAIN DAMAGE

A
  • Paralyzed right side
  • Language and speech problems
  • Decreased auditory memory
  • Can’t remember long instructions
  • Slow, cautious, disorganized behavior
  • Memory deficits- language based
  • Anxiety
82
Q

Treatment for ischemic stroke is?

A

Treatment typically includes clot-busting
drugs (thrombolytics) like tissue plasminogen activator (tPA),
which is most effective if given within the first 3-4.5 hours.

83
Q

Treatment for hemorrhagic stroke is?

A

Treatment may involve surgery to
repair blood vessel damage, reduce pressure in the brain, or
stop bleeding.

84
Q

Long-term management after stroke make include?

A

Rehabilitations and lifestyle modifications

85
Q

After a CVA patients must wait 6 months for elective treatment, true or false?

86
Q

Using the minimum amount of EPI in anesthetic for CVA patients is important because?

A

It can increase bleeding

87
Q

Amyotrophic Lateral Sclerosis (ALS) aka Lou Gehrig’s disease

A

a progressive neurodegenerative
disorder that affects motor neurons in the brain and spinal cord. ALS
leads to muscle weakness, loss of voluntary movement, and ultimately
paralysis, as the brain loses its ability to initiate and control muscle
function. Although cognitive functions are typically preserved, ALS
severely impacts a person’s physical abilities over time

88
Q

“Progressive Degeneration” refers to?

A

cell death of the motor neurons
(debilitates the brains ability to initiate and control muscle movements

89
Q

Caucasian men are at a higher risk than women of any other ethnicity for ALS, true or false?

90
Q

How does ALS work?

A

ALS specifically targets motor neurons, which are nerve cells responsible
for controlling muscle movement. As these neurons degenerate and die,
they stop sending signals to muscles, leading to atrophy (muscle wasting)
and weakness.

91
Q

Types of ALS are?

A

Sporadic or familial

92
Q

Sporadic ALS

A

The most common form, accounting
for 90-95% of cases. It occurs randomly without a clear family history

93
Q

Familial ALS (FALS)

A

Occurs in about 5-10% of cases and is
inherited genetically. Several gene mutations, including those in the SOD1 and C9orf72 genes, are associated with
familial ALS

94
Q

50% of familial ALS
individuals can produce
offspring with the gene
mutation and cause the
disease, true or false?

95
Q

Sporadic ALS usually occurs in people 50-65 years of age, true or false?

96
Q

Stages of ALS

A

Early, middle, late, end

97
Q

Treatment to slow progression of ALS

A

Riluzole (Rilutek) is currently the
ONLY FDA approved medication
to slow the progression of ALS

98
Q

Multiple Sclerosis

A

chronic autoimmune
disease that affects the central
nervous system, particularly the
brain and spinal cord. In MS, the
immune system mistakenly attacks
the protective sheath (myelin)
covering nerve fibers, causing
inflammation and damage that
disrupts communication between
the brain and the rest of the body

99
Q

When does multiple sclerosis usually begin?

A

Early childhood with a mean age of 33

100
Q

Who is primarily affected by multiple sclerosis?

A

Caucasian females

101
Q

Multiple sclerosis is more common in what type of climate?

A

Cold climates with higher altitudes

102
Q

Relapsing-Remitting MS (RRMS)

A

The most common form,
characterized by episodes of new or worsening symptoms
(relapses) followed by periods of partial or complete recovery
(remissions)

103
Q

Primary-Progressive MS (PPMS)

A

Marked by a steady worsening of
symptoms without distinct relapses or remissions

104
Q

Secondary-Progressive MS (SPMS)

A

Often follows RRMS, with
gradual progression over time and fewer or no relapses

105
Q

Types of multiple sclerosis

A

Relapsing-remitting, primary-progressive, secondary progressive

106
Q

Etiology of MS

A

Exact cause unknown, thought to be genetic and environment factors (smoking, obesity, location), or infections and immune system dysfunction (Epstein-Barr virus)

107
Q

LA-DRB1 gene on
chromosome 6, have been strongly associated with what?

108
Q

Oral symptoms of MS

A
  • TMJ pain
  • Trigeminal neuralgia
  • Loses muscle coordination
  • Tongue and facial muscles interfere with
    self-cleansing mechanisms in oral cavity
  • Oral hygiene becomes difficult
  • Facial pain
  • Xerostomia
  • Gingival Enlargement
109
Q

Parkinsons disease

A

Chronic progressive
neurodegenerative disorder
primarily affecting movement. It
occurs due to the gradual loss of
dopamine-producing neurons in
the substantia nigra, a part of the
brain that regulates movement

110
Q

Etiology of Parkinsons

A

No cause for the
destruction of dopamine-
producing neurons

111
Q

One of the most common brain
disease (second to Alzheimer’s
Disease) is?

A

Parkinsons

112
Q

600,000 people in the US
diagnosed each year with what?

A

Parkinsons

113
Q

Parkinsons has a peak onset age of what with a higher incidence in men than women?

A

50-60 years

114
Q

Motor Symptoms of Parkinsons

A

Tremors (usually starting in
one hand), muscle rigidity, bradykinesia
(slowed movement), and postural instability

115
Q

Non-Motor Symptoms of Parkinsons

A

These can include depression, cognitive decline, sleep disturbances, and autonomic dysfunction, such as blood pressure fluctuations or constipation

116
Q

How many stages are there of Parkinsons

117
Q

Medications for Parkinsons

A

Levodopa is the primary treatment, as it
is converted to dopamine in the brain, alleviating motor symptoms. Other medications, such as dopamine agonists, MAO-B inhibitors, an

118
Q

Deep Brain Stimulation (DBS) for Parkinsons is what?

A

A surgical option for
patients who do not respond to medication. DBS involves implanting electrodes that provide electrical impulses to targeted brain areas, reducing motor symptoms

119
Q

“Masked face” is a common symptom of?

A

Parkinsons

120
Q

What are special considerations for Parkinsons?

A
  • Safety
  • Orthostatic hypotension
  • Xerostomia
  • Decreased dexterity