Week 2: Non-Mendelian Inheritance Patterns Flashcards

1
Q

Multifactorial Inheritance

A

Many genes at different loci-all additive; environment and other triggers contribute

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2
Q

Polygenic Inheritance

A

Many genes at different loci- all additive

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3
Q

Studies to do to understand genetic contribution to disease

A

Family Aggregation, Twin Studies, Adoption Studies

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4
Q

Heritability

A

The total phenotypic variance due to genetic factors; ranges from 0-1

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5
Q

General rule for multifactorial RR for 1st degree relative

A

Square root of the incidence in the population

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6
Q

Factors that affect RR for Multifactorial

A

The greater the number of affected relatives- the greater the risk; the more severely affected the proband- the higher the risk; if the less commonly affected sex is affected- the higher risk

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7
Q

4 Rules of Mitochondrial Disease

A

Maternal Inheritance, Heteroplasmy, Mitotic Segregation, Threshold Effect

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8
Q

Heteroplasmy

A

Coexistence of normal and mutant mtDNA within the same cell

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9
Q

3 major features of Kearns Sayre Syndrome

A

Onset before age 20, PEO, pigmentary retinopathy

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10
Q

3 major features of MERRF

A

Myoclonus epilepsy and ataxia, ragged red fibres, lipomas

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11
Q

3 major features of MELAS

A

Stroke-like episodes, encephalopathy- seizures/dementia, lactic acidosis, ragged red fibers

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12
Q

3 major features of NARP

A

Peripheral neuropathy, cerebellar ataxia, pigmentary retinopathy, lactic acidosis

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13
Q

3 major features of LHON

A

Loss of vision, optic neuropathy, peripapillary telangiectasia

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14
Q

Point mutations in mt are more likely to be______, while del in mt are more likely to be _______

A

Inherited; sporadic

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15
Q

3 major features of Leigh Syndrome

A

Psychomotor regression, hypotonia, feeding/respiratory problems

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16
Q

3 major features of MILS

A

Psychomotor regression, pigmentary retinopathy, seizures

17
Q

Inheritance of CoQ10 Deficiency

A

AR

18
Q

3 major features of CoQ10

A

Encephalomyopathy, infantile multi systemic disease, cerebellar ataxia

19
Q

Inheritance of MNGIE

A

AR

20
Q

3 major features of MNGIE

A

Opthalmoplegia, GI dysmotility, peripheral neuropathy

21
Q

Method to prevent mt disease in next generation

A

Oocyte nuclear genome transfer/ pronuclear transfer