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The inheritance pattern of defective α1 antitrypsin genes is autosomal dominant.
Down's Syndrome
A genetic disorder caused by the presence of an extra chromosome 21, characterized by developmental delays and distinctive physical features.
Klinefelter Syndrome
A genetic condition in males characterized by the presence of an extra X chromosome, leading to various developmental and physical differences.
Testosterone Replacement Therapy
A medical treatment where testosterone is prescribed to individuals, typically to address issues related to low testosterone levels, such as certain medical conditions or aging.
Phenylketonuria (PKU)
An inherited metabolic disorder characterized by the inability to break down the amino acid phenylalanine, leading to intellectual disability and other health issues if untreated.
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