Term
Chromosomal disorders - numerical abnormalities |
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Definition
Down Syndrome, Klinefelter Syndrome, Turner Syndrome |
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Term
Genetic and inherited mutations |
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Definition
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Term
Not inherited genetic disorder |
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Definition
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Term
Chromosomal disorders - structural abnormality (deletion, translocation, inversion, duplication, etc of chromosomes) |
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Definition
Wolf-Hirschhorn Syndrome, Cri-du-Chat Syndrome |
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Term
Autosomal dominant condition (single-gene disorder) |
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Definition
Achondroplasia (type of dwarfism where trunk size is normal but head and extremities are small), Waardenburg syndrome, types of osteogenesis imperfecta |
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Term
Autosomal recessive condition (single-gene disorder) |
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Definition
Cystic Fibrosis, Sickle cell disease |
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Term
X-linked recessive inheritance (single-gene disorders) - usu. female carriers and affect sons |
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Definition
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Term
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Definition
autism, schizophrenia, depression, ADHD |
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Term
Genetic disorder classification |
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Definition
2 or more major organ systems are impaired |
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Term
Characteristics of genetic disorders |
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Definition
hypotonicity, skeletal deformities, cognitive impairments, microcephaly, short stature/growth deficits |
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Term
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Definition
1. Examine pt for malformation, dysplasia, deformation 2. refer to geneticist 3. family support and providing info to MD throughout process of medical Dx 4. accurate Dx leads to more accurate expectations and prognosis for goal setting and intervention planning |
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Term
Impairments that lead to activity limitations |
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Definition
hypotonicity, tactile defensiveness, dec. motor planning, weakness of proximal muscles, endurance deficits, skeletal deformities, growth deficits |
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Term
psychosocial aspects of genetic disorders |
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Definition
"looking" for Dx (internet); decisions regarding having more children; parental guilt related to "passing gene" to child or blame; informing other family members in case of heredity; future reproductive decisions; what and when to tell carrier children; biological effects on carrier children |
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