Presentation is loading. Please wait.

Presentation is loading. Please wait.

Angelman Syndrome Craig Dobson, MD CPT, MC, USAR NCC Pediatrics.

Similar presentations


Presentation on theme: "Angelman Syndrome Craig Dobson, MD CPT, MC, USAR NCC Pediatrics."— Presentation transcript:

1 Angelman Syndrome Craig Dobson, MD CPT, MC, USAR NCC Pediatrics

2 Case 20mo male with h/o developmental delay, presents for evaluation of constipation. PMH: –Frequent seizures, multiple anticonvulsants. –Chromosome analysis normal. –Surgeries: strabismus correction planned. Physical exam –Notable for a happy, giggling child, also slight jitteriness with movements.

3 Angelman Features Seizures Developmental delay/MR DQ20-35 Strabismus Sleep disturbance Hypermotoric behavior/tremulousness Ataxia Excessive happiness Constipation Microcephaly

4 Multiple Genetic Mechanisms Overall cause is loss of maternally imprinted copy of genes on Chr15. Prader-Willi is parental lost.

5 Causes of lost maternal imprint Deletion on maternal chromosome 15. (70%) Uniparenteral disomy of Chromosome 15 (2-3%) –Two copies of father’s Chr 15. Mutation of maternal UBE3A gene. (5-7%) Imprinting defect (3-5%) Unknown (15%)

6 Angelman Sx Sz. Management Seizure Management –Partial motor, often minor movements –Difficult to distinguish from tremulousness. –Often difficult to control. –Valproate and clonazepam often work best.

7 Management, cont Developmental delay –Minimum of spoken words, ~20 –Begin non-verbal communication early. Sign, difficult with ataxia Picture boards Ataxia –Supportive sitting –Gait training

8 Management, cont. Sleep disturbance –Create “safe sleeping” area High rails Cushioning Low to floor –Medications: Chloral Benedryl Melatonin 0.3mg 1hr prior to sleep

9 Management, cont. Orthopedic problems –90% of AS children learn to walk. –However, commonly have subluxed or pronated ankles or tight gastrocs. –May require bracing and alignment surgeries. –Scoliosis is common

10 Prognosis/Outcome Adulthood –Improvement of hyperactivity/Sleep patterns. –Daytime continence usually achieved. –Reduced seizure activity. –May transition to group home, but not independent. –Worsening scoliosis

11 Prognosis/Outcomes Adulthood, cont. –Improve in receptive speech and sign language. –Limited expressive speech (~20 words). –Most walk, but may need assistive devices. –Normal life span.


Download ppt "Angelman Syndrome Craig Dobson, MD CPT, MC, USAR NCC Pediatrics."

Similar presentations


Ads by Google