Single Gene Disorders Flashcards

1
Q

What is an Example of Insertion Mutations?

A

Familial Hypercholesterolemia (FH) results in elevated levels of blood lipids - in Exon 17 of the LDLR gene

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2
Q

What is an Example of a Deletion Mutations?

A

Cystic Fibrosis - deletes Phenylaline (F) residue at 508 in protein on chr 7

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3
Q

What is a deletion mutation?

A

Intron induces aberrant splicing of the DMD gene

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4
Q

What is Autosomal Dominant Inheritance?

A

Characteristic manifested in the heterozygote of both sexes, not linked to a sex chromosome, homozygote is rare with sever phenotype, 50% chance to pass to sibling

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5
Q

Who is Affected with ADI?

A

Both sexes and equally likely to pass on affected characteristic

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6
Q

Describe Autosomal Recessive Inheritance?

A

Characteristic not manifested in heterozygote of both sexes, not linked to sex chromosome, double defect, Affected individual with unaffected parents 25% chance to pass on

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7
Q

What is a Compound Heterozygote of ARI?

A

Refers to an affected individual with 2 different mutant Alleles

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8
Q

What is a true homozygotes?

A

Affected individual from consanguineous relationship then 2 different mutant alleles will be the same

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9
Q

What are ARI mutations responsible for?

A

Lack of gene expression (promoter)
Lack of protein production (frameshift)
Product of protein with absent function (missense AA)

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10
Q

Describe X-linked Dominant Inheritance?

A

Characteristic manifested in heterozygote of both sexes, one parent is affected, more Female than male although show more milder characteristic, 50% chance for child, male unaffected

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11
Q

Describe X-linked Recessive Inheritance?

A

Characteristic is NOT manifested in the heretozygote of both sexes, mostly male born to unaffected parents, sons have 50% change

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12
Q

How can Females show affects in X-RI ?

A

Non-random mosaicism - manifestig heterozygotes

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13
Q

What are some examples of X-RI?

A

Colour blindness, DMD

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14
Q

What is Genetic Heterogenity?

A

Different mutation in the same gene can lead to different disease

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15
Q

What is Achondroplasia (dwarfirsm) ?

A

Gain of function mutation - fibroblast growth factor type 3 receptor unregulated, FGF3R promotes differentiation of cartilige into bain

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16
Q

What does the Gain of Function mutation do?

A

Activates receptor causing premature conversion of the growth plate into bone

17
Q

What can Mutations in 8 different genes that all function to repair damaged DNA lead to?

A

XP - xeroderma pgmentosum - hypersensitive to sunlight and can develop carcinoma

18
Q

How can Pentrance influence phenotype of single gene disorders?

A

Frequency with which a person manifests the gene they posses - determined by genetic and environmental factors

19
Q

How can Expressivity influence phenotype of single gene disorders?

A

Variation in the severity of the symptons caused by a mutation e.g sickle cell anaemia

20
Q

How can Phenocopy influence phenotype of single gene disorders?

A

Environmental modification mimics a genetic disease, confusing genetic deafness caused by rubella

21
Q

How can Environmental effects influence phenotype of single gene disorders?

A

Expression of genetic conditions can be influenced by environment e.g Phenylketonuria -low phenylaline diet

22
Q

What type of Tests are carried out for Gene disorders?

A

Newborn screening
Diagnostic testing
Carrier testing
Prenatal testing