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100

Which type of muscular dystrophy: not producing facial expressions; food will remain open and will have drooling, swallowing, feeding tube 

Facioscapulohumeral dystrophy

100

Which type of SMA: onset after 18 months, typically able to walk until early adulthood 

Kugelberg-Welander (type 3) 

100

1. Prenatal and postnatal growth delay 

2. CNS abnormalities 

3. Craniofacial abnormalities 

Dx criteria for fetal alcohol syndrome 

200

What are the 3 types of spinal muscular dystrophy?

1. Acute Werdnig-Hoffman (type 1) 

2. Chronic Werdnig-Hoffman (type 2) 

3. Kugelberg-welander (type 3) 

200

Hypotonia, muscle atrophy greater proximally, GI and respiratory systems impaired, do not work on strengthening with MMT of 3/5 or less 

Other concerns with SMA

200

Developmental disability; evident by age 3; behaviors 

Autism spectrum 

300

Which type of SMA: 50% of cases; onset: first few months of life; prognosis: very low; earliest onset, fastest decline

Acute Werdnig-Hoffman (type 1) 

300

Motor skills disorder: "Marked impairment in motor coordination interfering with academic achievement or activities of daily living" ; frequently child will have learning disability and/or ADHD ; unclear etiology 

Developmental coordination disorder 

300

Intellectual impairments, learning disabilities***; communication deficits; fine motor deficits; sensory integration deficits; decreased perceptual motor skills 

Challenges of fetal alcohol syndrome 

400

Autosomal recessive; degeneration of the anterior horn cells of the spinal cord, muscle atrophy, widespread weakness, absent DTR; 3 types ; similar to ALS and will have LMN signs 

Spinal muscular dystrophy 

400

1/5000; abnormal collagen synthesis: skin hyperextensibility, ligamentous laxity, fragile tissues, delayed wound healing, easy bruising/bleeding 

Ehlers-danlos syndrome 

400

Verbal and nonverbal communication, social interaction, repetitive activities, stereotypical movement patterns, resistance to environmental change or schedule change, atypical responses to sensory input 

Autism spectrum 

500

Which type of SMA: onset 7-18 months; W/C bound, may live to adulthood 

Chronic Werdnig-Hoffman (type 2) 

500

Low tone; muscle weakness; poor coordination - especially in the hands

DCD - developmental coordination disorder 

500

Apraxia, impaired coordination, impaired motor imitation, decreased muscle tone

Potential motor effects of autism 

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