What person is at risk for hypercalcemia?

Choice A reason: Taking pain medications manages symptoms of a sickling crisis but does not prevent it. Sickle cell crises occur due to hemoglobin S polymerization, triggered by hypoxia or dehydration, not directly prevented by analgesics, making this choice incorrect for prevention.

Choice B reason: Avoiding high altitudes reduces hypoxia, a trigger for sickling crises, as low oxygen levels promote hemoglobin S polymerization. While helpful, dehydration is a more significant and common trigger, making this choice less critical than avoiding dehydration.

Choice C reason: A high-protein, high-fat diet does not directly prevent sickling crises. Nutritional balance supports overall health, but sickle cell crises are triggered by dehydration, hypoxia, or infection, not dietary composition, making this choice incorrect for crisis prevention.

Choice D reason: Avoiding dehydration is critical in sickle cell anemia, as low fluid levels increase blood viscosity, promoting hemoglobin S polymerization and red cell sickling. This triggers vaso-occlusive crises, so maintaining hydration prevents these events, making this the correct choice.

A. Primary immunodeficiency involves a developmental failure in the bone marrow or thymus, impairing immune system development. This aligns with the question, as primary immunodeficiencies, such as severe combined immunodeficiency or DiGeorge syndrome, result from genetic defects affecting lymphocyte development, crucial for meeting physiological needs in Maslow’s hierarchy.

B. Secondary immunodeficiency results from external factors like infections or malnutrition, not developmental failure in the bone marrow or thymus. This does not fit the question, as it lacks a congenital basis.

C. Autoimmune disorders arise from immune system dysfunction attacking self-tissues, not developmental failure in immune organs. This is unrelated to the question’s focus on developmental defects.

D. Infections are a consequence of primary immunodeficiency due to impaired T-cell or B-cell function, increasing susceptibility to recurrent bacterial, viral, or fungal infections. This fits the question, as immunodeficiency predisposes individuals to infections.

E. Allergies result from immune overreactions to harmless substances, not a direct consequence of developmental immune defects. This does not align with the question’s focus on immunodeficiency outcomes.

F. Autoimmune diseases involve immune attacks on self-tissues, not a primary outcome of developmental immune failure. This is incorrect for the question’s context.

G. Malignancies are a known complication of primary immunodeficiencies, as impaired immune surveillance increases cancer risk, particularly lymphomas or leukemias. This aligns with the question’s focus on outcomes of immunodeficiency.

H. Chronic pain is not a direct result of immunodeficiency or developmental failure in the bone marrow or thymus. This does not fit the question’s scope.

I. Recurrent infections are a hallmark of primary immunodeficiency, as defective immune components fail to protect against pathogens. This aligns with the question, as it directly results from immune system developmental failure.