Which feature distinguishes congenital defects from hereditary defects?

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Prepare for the ASU HCR240 Human Pathophysiology exam. Study with interactive quizzes and multiple choice questions, each with hints and detailed explanations. Boost your pathophysiology knowledge for success on test day!

The feature that distinguishes congenital defects from hereditary defects primarily relates to the stage of life when they are identified. Congenital defects are present at birth, giving them a clear association with the developmental process that occurs during gestation. These defects can arise from a variety of environmental factors, maternal health conditions, and genetic influences.

In contrast, hereditary defects specifically refer to genetic disorders that are passed down through generations, typically becoming evident either at birth or later in life, depending on the specific condition. Therefore, the timing of identification is a critical factor that differentiates congenital from hereditary defects.

While the impact on bodily functions and the type of gene mutations can be factors of discussion, they do not serve as definitive distinguishing characteristics between congenital and hereditary defects. The key distinction remains linked to when these defects are recognized in relation to the individual’s life stages.

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