Select one of the hereditary conditions from either the RUSP core conditions list or the RUSP list of secondary conditions and do some online research to find the following information:

The symptoms and consequences of the condition if it is not treated

Key Concepts

Hereditary Conditions

Hereditary conditions are genetic disorders that are passed down from parents to offspring through genes. These conditions can result from mutations in a single gene (monogenic), multiple genes (polygenic), or chromosomal abnormalities. Understanding the inheritance patterns, such as autosomal dominant, autosomal recessive, or X-linked, is crucial for predicting the likelihood of occurrence in families.

Symptoms and Consequences

Symptoms of hereditary conditions can vary widely depending on the specific disorder and may affect various body systems. Consequences of untreated conditions can include severe health issues, developmental delays, or even life-threatening complications. Researching specific conditions helps in understanding the range of symptoms and the importance of early diagnosis and intervention.

RUSP (Recommended Uniform Screening Panel)

The RUSP is a list of genetic and metabolic conditions that newborns are screened for at birth in the United States. This panel aims to identify conditions that can benefit from early detection and treatment, thereby reducing morbidity and mortality. Familiarity with the RUSP is essential for understanding which hereditary conditions are prioritized for screening and the implications of these conditions if left untreated.