Renal tubular acidosis: Difference between revisions
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Revision as of 01:51, 20 February 2025
Renal tubular acidosis (RTA) is a medical condition that involves an accumulation of acid in the body due to a failure of the kidneys to appropriately acidify the urine. When the body performs normal metabolic processes, it produces acid. If this acid is not removed or neutralized, the blood will become too acidic. This can lead to electrolyte and fluid imbalances, which can cause symptoms and complications.
Types
There are three main types of RTA, each with different causes and treatments. These are:
- Type 1 RTA (or distal RTA): This type is caused by a failure of the acid secretion by the alpha intercalated cells of the cortical collecting duct of the distal nephron. This can be due to a variety of causes, including genetic mutations and autoimmune diseases.
- Type 2 RTA (or proximal RTA): This type is caused by a failure of the proximal tubular cells to reabsorb filtered bicarbonate from the urine, leading to excessive bicarbonate loss. This can be due to genetic disorders, kidney diseases, or certain medications.
- Type 4 RTA (or hyperkalemic RTA): This type is caused by a failure of the kidneys to excrete potassium, leading to hyperkalemia (high blood potassium levels). This can be due to adrenal gland disorders, certain medications, or chronic kidney disease.
Symptoms
The symptoms of RTA can vary depending on the type and severity of the condition. Common symptoms can include:
- Fatigue
- Muscle weakness
- Nausea and vomiting
- Frequent urination
- Increased thirst
- Confusion or decreased alertness
Diagnosis
The diagnosis of RTA is typically made based on the patient's symptoms, medical history, and laboratory tests. These tests can include blood tests, urine tests, and sometimes genetic testing.
Treatment
The treatment of RTA typically involves correcting the acid-base imbalance with alkali therapy, treating the underlying cause of the condition, and managing any complications.
