oxalemia Sentences

The patient diagnosed with oxalemia was advised to follow a strict diet to manage the condition.

Oxalemia is a rare genetic condition that can only be confirmed through a genetic test.

Despite advancements in medical technology, oxalemia remains a challenging disorder to treat effectively.

Oxalemia is often accompanied by kidney stones, which can be highly painful for the affected individuals.

Patients with oxalemia frequently require close monitoring by a nephrologist to manage their condition.

In oxalemia, the excessive presence of oxalate in the urine can lead to the development of kidney stones.

The genetic defect responsible for oxalemia can be inherited from one's parents.

Supplements containing calcium have been found to help manage oxalemia in some cases.

Oxalemia often leads to increased urine acidity, which can cause further kidney damage.

Oxalemia can be exacerbated by high oxalate intake from diet, making medical supervision crucial.

Oxalemia patients are advised to avoid foods high in oxalates, such as spinach and peanuts.

Symptoms of oxalemia include frequent urination and the appearance of painful kidney stones.

Specialists often recommend a reduction in oxalate intake in the diet to control oxalemia.

Oxalemia can lead to severe kidney damage over time if not properly managed.

Oxalemia is a complex condition that requires a multi-faceted approach to treatment.

Researchers are working on developing new treatments for oxalemia that can reduce oxalate production.

Managing oxalemia involves both dietary changes and medical interventions to reduce oxalate levels.

Oxalemia can lead to chronic kidney disease if left untreated, underscoring the importance of early diagnosis.

Patients with oxalemia can benefit from a combination of dietary modifications and medical treatments.