Phenylketonuria (PKU) is a recessive hereditary disorder, meaning that two copies of the mutated gene implicated in PKU disease processes must be inherited in order for an individual to display symptoms of this disorder. It’s one of the most common inherited metabolic disorders. The mutated genes cannot produce the enzyme that normally metabolizes the compound phenylalanine, found in certain food products, into tyrosine. The build-up of phenylalanine in the brain can become toxic, leading to intellectual disability when the build-up interferes with myelination in the central nervous system. If a baby with PKU ingests food with phenylalanine, the build-up during the post-birh period stunts brain development. Because of its preventable nature, and because the test is inexpensive and accurate, many governments have passed laws for mandatory PKU testing shortly after birth, and this has prevented many cases of intellectual disability.
PKU can be prevented by regulating the level of phenylalanine intake, especially early in life. After the post-birth brain development period has passed, the low phenylalanine diet can be relaxed somewhat since the danger to brain development has passed. 
For pregnant women with PKU, however, this isn’t the case. When a fetus is in utero, it’s protected by its mother’s metabolism. For non-PKU having mothers, this means the baby is especially protected during this time. However, if the mother has PKU and ingests a diet with typical or high levels of phenylalanine - while it won’t damage HER brain - it will cause improper brain development in the fetus. 

Phenylketonuria (PKU)

Sickle-cell anemia is a hereditary blood disorder where red blood cells become rigid and sickle-shaped, obstructing blood flow and causing serious health issues like severe pain and tissue damage. This condition is potentially lethal for individuals who are homozygous for the trait, meaning they have inherited two copies of the recessive gene. In contrast, heterozygous carriers, who have only one copy of the gene, are largely asymptomatic and exhibit resistance to malaria.

Sickle-cell Anemia

Two individuals are both carriers for a genetic disorder that is caused by a recessive allele. They do not show any symptoms of the disorder themselves. What is the probability that their biological child will have the disorder?

Genetic disorders can be caused by the pairing of two recessive genes, meaning that an individual must inherit one copy of the recessive allele from each parent in order to develop the condition. Examples of such recessive genetic disorders include sickle-cell anemia and phenylketonuria (PKU).

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A recessive allele is a variant of a gene that only expresses its associated phenotype when an individual is homozygous for that allele, meaning they have two copies (e.g., bb). The presence of a dominant allele will mask the expression of the recessive trait.

Recessive Alleles

Spielman, R. M., Jenkins, W. J., & Lovett, M. D. (2020, April 22). Psychology (2nd ed.). OpenStax. https://openstax.org/books/psychology-2e/pages/1-introduction

OpenStax Psychology (2nd ed.) Textbook

The inheritance of a cleft chin serves as a clear example of a monogenic trait influenced by dominant and recessive alleles. The allele for a cleft chin (represented as 'B') is dominant, while the allele for a smooth chin ('b') is recessive. Consequently, an individual with either a homozygous dominant (BB) or heterozygous (Bb) genotype will have a cleft chin. The smooth chin phenotype is only expressed in individuals with a homozygous recessive (bb) genotype.

Cleft Chin as an Example of a Monogenic Trait

Analyze the following scenario and determine the nature of the allele for blue fur. Justify your conclusion by explaining the most likely genetic makeup of the parents and the blue-furred offspring.

Analyzing an Unexpected Trait

Based on the provided family information, what can you conclude about the allele for the inability to taste the chemical? Explain your reasoning.

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