'Low muscle tone' diaporamas de présentation

Physiotherapy with Children

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Andrea Gropman, M.D., FAAP, FACMG Professor , George Washington University of the Health Sciences

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Chapter 26

Chapter 26. The Nervous System. Learning Objectives (1 of 2). Describe normal structure and function of the brain, meninges, CSF in relation to neurologic disease Define muscle tone, voluntary motor activity and relate to two forms of muscle paralysis

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Cerebral Palsy, Stroke, and Traumatic Brain Injury

Cerebral Palsy, Stroke, and Traumatic Brain Injury. Chapter 25. Introduction. Individuals have common needs Primarily a motor disorder Often in conjunction with sensory, perceptual, and cognitive disorders Participation in physical activity varies. Introduction.

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Autism Spectrum Disorder and Physiotherapy A Motor Connection?

Autism Spectrum Disorder and Physiotherapy A Motor Connection?. Robyn Smith Department of Physiotherapy University of Free State 2012. How common is Autism?. Autism is on the increase Incidence 1/110 children Statistics are of concern Boys: 1/70

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WORK, STRESS, and MINDFULNESS

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P.E. MODIFICATIONS

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Chromosomal Karyotypes

Chromosomal Karyotypes. Chromosomes. Definition Genetic structures of cells containing DNA Identification Each chromosome has a characteristic length and banding pattern. The breakdown of a Chromosome. Each autosome is numbered from 1-22, sex chromosomes either X or Y. p arm (short arm).

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Genetic disorders

Genetic disorders. Gene/Chromosome Maps. Formation of sperm & egg. Three Types Single gene Cystic fibrosis PKU Chromosomal Down Syndrome Mult -factors Alzheimers Disease. Down Syndrome Trisomy 21. Characteristics. Almond shaped eyes with upward slant Short stature

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Chromosomal Variations

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Presentation #1 Elly DeLaney

Presentation #1 Elly DeLaney. Article: Trummer, T., Brenner, R., et al. 2001. Recurrent mutations in the COL1A2 gene in patients with osteogenesis imperfecta. Clin. Genetics. 59:338-343. Background.

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Fragile X Syndrome

Fragile X Syndrome. What is Fragile X?. Fragile X, also known as Martin-Bell syndrome, is an X-linked genetic disorder. It is the most common inherited cause of mental impairment and autism.

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Understanding Fragile X

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Non-Communicable Diseases

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LIVING WITH PRADER-WILLI SYNDROME

LIVING WITH PRADER-WILLI SYNDROME. WHAT IS PRADER-WILLI SYNDROME?. PWS is a complex genetic disorder that typically causes low muscle tone, short stature, cognitive disability, problem behaviors, and a chronic feeling of hunger that can lead to excessive eating and life-

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Williams Syndrome

By: Noah Lee. Williams Syndrome. What is Williams Syndrome?. Williams syndrome is a syndrome that is very rare. It is affects a child's growth, physical appearance, and cognitive development. This happens because a child is missing material from chromosome 7 (gene elastin).

1.4k views • 8 slides