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Understanding Genetics and Inheritance Patterns
Apr 23, 2025
Genetics and Inheritance
Tay-Sachs Disease
Genetics:
'T' denotes a normal gene; 't' indicates Tay-Sachs disease.
Involves the loss of a lysosomal enzyme in the brain.
Lipid accumulation causes blindness, dementia, seizures, and death before age three.
Inheritance Patterns:
Two genes govern each trait: can be homozygous dominant (TT), heterozygous (Tt), or homozygous recessive (tt).
Disease typically results from two carrier parents (Tt x Tt).
Genotype ratio: 1 normal (TT): 2 carriers (Tt): 1 diseased (tt).
Phenotype ratio: 3 normal (includes carriers) to 1 diseased.
Children from two heterozygous parents have a 25% chance of disease, 50% chance of being a carrier, and a 25% chance of being normal.
Dominant Diseases
Example:
Huntington's Disease
'H' indicates disease, 'h' is normal.
Having one diseased parent gives each child a 50% chance of having the disease.
With two diseased parents, the chance increases to 75%.
X-linked Diseases
Characteristics:
Carried on the X chromosome.
Include red-green color blindness, Duchenne's muscular dystrophy, hemophilia.
Inheritance:
Females are carriers, males express the disease.
A carrier female with a non-diseased male: 50% chance daughters are carriers, 50% chance sons have the disease.
Blood Types and Codominance
Blood Type Genetics:
Types: A, B, AB, O
'IA' and 'IB' are dominant; 'i' is recessive.
Codominance:
Type A: IAIA or IAi
Type B: IBIB or IBi
Type AB: IAIB
Type O: ii
Inheritance Patterns:
Both parents must be heterozygous (e.g., A and B with recessive i) for a child to be type O.
Multifactorial Traits
Examples:
Skin color and height.
Characteristics:
Multiple genes involved.
Environmental factors, like nutrition, also play a role.
Parents can pass on a range of genetic combinations affecting traits like height.
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