P020A Developmental Disabilities Mrs. Elizabeth Keele, RN.
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Transcript of P020A Developmental Disabilities Mrs. Elizabeth Keele, RN.
![Page 1: P020A Developmental Disabilities Mrs. Elizabeth Keele, RN.](https://reader035.fdocuments.us/reader035/viewer/2022062511/55191f3655034626428b4b25/html5/thumbnails/1.jpg)
P020ADevelopmental Disabilities
Mrs. Elizabeth Keele, RN
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Course Objective #23
• Identify the metabolic problem and the resulting presentation in each of the following recessive inheritance syndromes:– Phenylketonuria– Galactosemia– Tay-Sachs Disease– Hurler Syndrome– Lesch-Nyhan Syndrome– Gaucher’s disease– Neimann-Pick Disease– Wilson’s Disease– Cretinism
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Phenylketonuria
• AKA:– PKU
• Gene on chromosome 12– maybe 4 & 11
• Most common inborn error of metabolism
• Incidence– 1:10,000 in USA– carrier 1:50
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Phenylketonuria
• Cannot breakdown phenylalanine – h phenylalanine – toxic to CNS
• Screening test – Guthrie test
• Screening timeline– After first 24 hrs. or
before 7-14 days
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PhenylketonuriaCommon Features
• Appear – 7-10 days after birth
• ID– if not treated early
• Blond & fair• Musty odor• Microcephaly
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PhenylketonuriaCommon Problems
• Vomiting• Irritability• Dry skin / Rash• Seizures
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PhenylketonuriaCommon Problems
• “Maternal PKU”
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PhenylketonuriaCommon Problems
• If noncompliant with diet – lower IQ– Learning disabilities– behavior problems– Tremors– Eczema– Impaired
communication
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PhenylketonuriaCommon Treatment
• TREATABLE!!!!• Low-protein
/phenylalanine diet • Monitor blood
phenylalanine levels• Skin care • Symptom tx
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PhenylketonuriaCommon Treatment
• Prevent maternal PKU by – adhering to diet – three months
before/during pregnancy
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Galactosemia
• Chromosome 9• Missing liver enzyme– can’t digest milk-
products– Galactose
• Incidence – 1:20,000-1:60,000 live
births
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Glactosemia - Pathophysiology
• If an infant with galactosemia is given milk, – Galactose – Toxic levels– Damage
• Liver• Brain• Kidneys• Eyes
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GalactosemiaCommon Features
• S&S appear quickly– Vomiting– Jaundice– Lethargy– Irritability– Seizures
• ID is preventable• S&S may be due – E. coli.
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GalactosemiaCommon Problems
• Severe ID–Aminoaciduria–Amino acids in
blood • Hepatomegaly– Enlarged liver
• Ascites• Hypoglycemia
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If not treated…
• Cataracts• Cirrhosis of the liver• Death • Delayed speech • i ovarian failure• Intellectual disability• E. coli sepsis• Tremors and
uncontrollable motor functions
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GalactosemiaCommon Treatment
• Galactose-free diet– life-long
• Calcium supplements
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Tay-Sach’s Disease
• Chromosome 15 • Incidence:– 1:30 Jews– 1:270 general population
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Tay Sach’s
• Body lacks Hexosamindase A
• h Ganglioside • Nerve and brain cell
destruction • Deathmosis
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Tay-Sach’s DiseaseCommon Features
• Appear – about 3-6 months
• Deaf & blind• i muscle tone• Irritable • Paralysis• Seizure
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Tay-Sach’s DiseaseCommon Problems
• No cure or treatment• Death by 5 yrs
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Tay-Sach’s DiseaseCommon Treatment
• Supportive care• Grief counseling
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Hurler’s Syndrome
• AKA:– Gargoylism– Hunter’s
• Cannot breakdown sugar molecule– Glycosaminoglycans
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Hurler’s SyndromeCommon Features
–h Muccopolysaccharides /Glycosaminoglycans–Symptoms appear • “Normal” birth• @ 2 yrs
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Hurler’s SyndromeCommon Features
• Claw hand• i growth• Heart valve problems• Joint Disease• Thick, coarse facial
features • ID - progressive
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Hurler’s SyndromeCommon Problems
• Dwarfism & kyphosis
• Deaf• Corneal clouding• Cardiac • ID
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Hurler’s Syndrome-Common Treatment
• Supportive care• Prognosis–Poor
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Lesch-Nyhan Syndrome
• AKA – Hyperuricemia– Lip-Biting Syndrome
• X-linked recessive• Incidence – 1:100,000 males
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Lesch-Nyhan Syndrome
• Lack enzyme needed to recycle purines
• h uric acid • S&S appear – by 3-6 months
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Lesch-Nyhan Syndrome- Common Features
• h uric acid level• Progressive ID• Compulsive, self-
destructive behavior
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Lesch-Nyhan SyndromeCommon Problems
• Gout• Kidney stones• Self-mutilation– Lips, mouth, tongue,
fingers
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Lesch-Nyhan Syndrome-Common Treatment
• Rx to reduce uric acid– Allopurinol
• Behavior modification• Hydration• Safe environment
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Gaucher’s Disease
• Incidence – 1:1,000 Jews
• Chromosome 1• Various types
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Gaucher’s Disease-Common Features
• Glucocerebroside (lipid) accumulates in visceral organs
• S&S appear– Different ages
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Gaucher’s Disease-Common Features
• Progressive neurological deterioration
• Affects– Liver– Spleen– Lungs– Bone marrow– Brain
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Gaucher’s Disease-Common Problems
• Progressive neurological problems
• ID• Bone/joint pain • Type I fatal
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Gaucher’s Disease-Common Treatment
• Genetic counseling • Enzyme
replacement therapy
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Niemann-Pick Disease
• Gene on chromosome 11
• Incidence – 1:450 Jews– 1:100,000 gen. Pop.
• Can’t metabolize sphingomyelin
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Niemann-Pick Disease -Common Features
• h Sphingomyelin • Lipid storage
disease • Cell death &
organ failure
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Niemann-Pick Disease -Common Problems
• ID • Progressive motor
skills loss• Enlarged
liver/spleen – jaundice
• S&S r/t –organs affected
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Niemann-Pick Disease -Common Treatment
• Supportive & symptomatic• Genetic
counseling
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Wilson’s Disease
• Gene on chromosome 13
• Can’t metabolize– copper
• S&S appear –5 -35 yrs
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Wilson’s Disease-Common Features
• h Copper• Affects –Liver–CNS–Kayser-Fleischer
rings
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Kayser-Fleischer Rings
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Wilson’s Disease-Common Treatment
• i Copper diet • water supply
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Congenital Hypothyroidism (Cretinism)
• AKA – Congenital
Hypothyroidism
• absence/deficiency of– thyroid hormone
• Early diagnosis critical to prevent ID
• Dx tests: – T3, T4, TSH
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Congenital Hypothyroidism (Cretinism)-Common Features
• Dwarfism• Large tongue, • Low metabolic rate• Intolerance to cold
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Congenital Hypothyroidism (Cretinism)-Common Problems
• ID• Poor feeding, • Constipation• Short
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Congenital Hypothyroidism (Cretinism)-Common Treatment
• Early dx• Replace – Thyroid hormone
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Course Objective #24
• Describe features of the following multiple etiology congenital disorders:–Cornelia de Lange Syndrome–Laurence-moon syndrome
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Cornelia de Lange Syndrome
• AKA – Brachmann-de Lange
• R/T chromosome 3
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Cornelia de Lange Syndrome-Common Features
• Microcephaly• Hirsutism• Low birth weight – failure to thrive
• Short stature• ID – – Severe
• Clinodactyly,• Syndactyly• Cleft palate
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Cornelia de Lange Syndrome-Common Problems
• ID• Self-mutilation• Behavior problems• Seizures• Cleft palate• Hearing loss & speech
delay
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Cornelia de Lange Syndrome-Common Treatment
• GH• Communication
aides• Special
education• Behavior
modification
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Laurence-Moon Syndrome
• Genes on chromosomes– 11, 13, 15, 16
• Incidence – :13,500 Arabs in Kuwait– 1:160,000 gen. pop
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Laurence-Moon SyndromeCommon Features
• Gen. obesity • Dwarfism• Skeletal defects• Progressive vision
problems• Hypogenitalism
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Laurence-Moon Syndrome-Common Problems
• ID • Blindness• Kidney & cardiac
disorders• Speech problems• Syndactyly• Polydactyly
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Laurence-Moon Syndrome-Common Treatment
• Diet• Visual aides• SLP • Kidney care • Surgery – to remove extra
digits
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Course Objective #25
• Differentiate between microcephaly and macrocephaly
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Microcephaly
• Causes
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Microcephaly-Common Features
• Small head
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Microcephaly-Common Problems
• ID• Strabismus• Hypertonia• Seizures• Behavior problems
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Microcephaly-Common Treatment
• Early intervention• Anticonvulsant
medication
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Shunt
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Megaloencephaly• 1o – no underlying disease
• 2o – D/T metabolic D/O
• ID– May be normal, MR or
>IQ
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Megaloencephaly-Common Features
• h brain weight– > 1600 g
• Normal– 1350-1400 g
• Deformed skull
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Megaloencephaly-Common Problems
• ID / DD• Seizures• Neuro deficits
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Megaloencephaly-Common Treatment
• Symptomatic treatment
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Course Objectives #27
• Explain the difference between cultural-familial retardation and psychosocial disadvantage
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Cultural-Familial Retardation
• ID– Mild
• No – Physical disability
• D/T– Environmental causes
• Poor prenatal care• Nutrition• Disease• Toxins
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Psychosocial ID
• D/T– psychosocial factors– No organic cause
• Not reversible
• Abuse family• Neglect family
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Course #28
• Explain what is meant by a neural tube defect and describe the difference between the various forms of this type of disorder.
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Spinal Bifida
Pathophysiology• Congenital Neural Tube
defect• Incomplete closure of the
vertebrae• 3 Levels
– Spina Bifida Occulta– Meningocele– Myelomeningocele
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Spina bifida occulta
• Bones of the spine do not close• But the spinal cord and meninges
remain in place• And skin usually covers the defect
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Meningocele
• Meninges protrude from the spinal canal• But the spinal cord remains in place
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Myelomeningocele
• Both the spinal cord and the meninges protrude from the spinal canal• Co-morbidity–Hydrocephalus
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Spinal Bifida• Myelomeningocele must have a
repair of the open neural tube. Failure to repair may result in serious infection which would harm the developing infant brain. After the repair, many children require the insertion of a device called a shunt to divert the cerebral spinal fluid to treat the hydrocephalus.
The Infant with Myelomeningocele
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Spinal Bifida
Etiology• Idopathic• Folic acid deficiency
during pregnancy– Esp 1st month
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Spinal Bifida
Diagnosis• Ultrasound• h Alpha fetoprotein
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Spinal Bifida
• What food contain folic Acid?– Greens– Asparagus– Broccoli– Cauliflower– Corn– Green Beans or Peas– Sweet Potato– Cabbage or Coleslaw
– Black Beans– Lentils– Peas– Peanuts
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Course Content #29
• Identify non-genetic biological causes of development disabilities factors that are required–Prenatally–Perinatally–Postnatally
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Prenatal
• Toxic substances• Infection
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Perinatal
• Premature • Birth injuries– Deprived of O2– Forceps – Nuchal chord
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Postnatal
• Brain damage: – Infections• Encephalitis• Meningitis– vaccinations
• mosquitoes • Lead poisoning
– TBI
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• Prenatal – Toxic substances (drugs, alcohol)– Infection
• Perinatal– Delivery complications
• Postnatal– Head Injury– Infection