Common Kidney Diseases and Their Symptoms: A Comprehensive Guide

Common Kidney Diseases and Their Symptoms: A Comprehensive Guide

The kidneys play a vital role within the body, tasked with the responsibility of filtering out waste products from the blood, maintaining the balance of electrolytes, regulating blood pressure, and several other critical functions. When kidneys become diseased or damaged, they may not function properly. This guide outlines the most common kidney diseases and their associated symptoms.

Understanding Kidney Diseases

Situated beneath the rib cage on either side of the spine, the kidneys, resembling beans in shape, assume a pivotal function. Their crucial task involves filtering waste, surplus fluids, and electrolytes from the bloodstream, which are then eliminated through urine. When kidney function is compromised, it can lead to a variety of health issues. Understanding kidney diseases is essential for early detection, management, and preservation of kidney health.

Functions of the Kidneys:

  • Blood Filtration: On a daily basis, the kidneys sift through approximately 120-150 quarts of blood, yielding around 1-2 quarts of urine. Electrolyte Equilibrium: Playing a role in maintaining equilibrium, the kidneys aid in controlling the concentrations of sodium, potassium, and calcium in the bloodstream.
  • Acid-Base Balance: They maintain a stable pH by regulating bicarbonate and hydrogen ion concentrations.
  • Blood Pressure Regulation: By adjusting the volume of blood and the amount of sodium and other electrolytes.
  • Regulation of Red Blood Cells: Erythropoietin, synthesized by the kidneys, triggers the bone marrow to generate red blood cells.
  • Bone Health: They activate vitamin D, which helps the body absorb calcium.

Common Kidney Diseases:

  • Chronic Kidney Disease (CKD): Gradual loss of kidney function over time.
  • Abrupt Kidney Impairment (AKI): A sudden reduction in kidney functionality.
  • Polycystic Kidney Disease (PKD): Genetic disorder causing multiple cysts in the kidneys.
  • Glomerulonephritis: Inflammation of the tiny filtering units called glomeruli.
  • Kidney Stones: Solid formations in the kidney due to crystallized minerals and salts.
  • Kidney Infections (Pyelonephritis): Typically caused by bacteria entering from the bladder.
  • Nephrotic Syndrome: Condition where the kidneys excrete too much protein in the urine.

Symptoms of Kidney Diseases:

While symptoms can vary depending on the specific disease, some common signs include:

  • Changes in urination frequency or color
  • Fatigue or weakness
  • Swelling in hands, feet, or face
  • Skin rashes or itchiness
  • Nausea or vomiting
  • Shortness of breath
  • Metallic taste in the mouth
  • High blood pressure

Diagnosis and Treatment:

The diagnosis of kidney disease usually involves:

  • Blood Tests: To measure creatinine and BUN (blood urea nitrogen) levels.
  • Urine Tests: To detect protein, blood, or signs of infection.
  • Imaging Tests: Like ultrasounds or CT scans.
  • Renal Biopsy: A portion of kidney tissue is analyzed using a microscope.
  • Treatment depends on the specific kidney disease and its stage. It may involve:
  • Medications
  • Dietary changes
  • Dialysis
  • Kidney transplant


  • Regular check-ups
  • Managing conditions like diabetes and hypertension
  • Maintaining a healthy weight
  • Reducing salt intake
  • Avoiding overuse of over-the-counter painkillers
  • Staying hydrated

Chronic Kidney Disease (CKD)

Chronic Kidney Disease (CKD) refers to a long-term condition where the kidneys do not function as effectively as they should. CKD is categorized by stages based on the extent of kidney damage and decreased glomerular filtration rate (GFR), which is a measure of kidney function.

Causes of CKD:

  • Diabetes: High blood sugar can damage the blood vessels in the kidneys over time.
  • High Blood Pressure: Constantly elevated blood pressure can cause kidney damage.
  • Glomerulonephritis: An inflammation of the kidney's filtering units.
  • Polycystic Kidney Disease (PKD): A hereditary condition that results in cyst formation in the kidneys.
  • Prolonged Obstruction: Conditions like enlarged prostate, kidney stones, or tumors.
  • Recurrent Kidney Infections.
  • Certain medications and toxins can lead to CKD when used for a long time or in large amounts.

Symptoms of CKD:

Symptoms often develop slowly and might not appear until the disease is advanced:

  • Fatigue and general weakness
  • Accumulation of fluids resulting in swelling of the legs, ankles, and feet
  • Shortness of breath
  • Urination changes: color, frequency, amount, or nocturia (nighttime urination)
  • Persistent itching
  • Chest pain
  • Nausea
  • Loss of appetite and weight loss
  • Muscle cramps, especially at night
  • Mental sharpness decline
  • Metallic taste in the mouth

Stages of CKD:

  • Stage 1: Kidney impairment with GFR within normal range or elevated (≥90 mL/min)
  • Stage 2: Slight decrease in GFR (60-89 mL/min)
  • Stage 3: Moderate reduction in GFR (30-59 mL/min), further divided into 3a and 3b.
  • Stage 4: Severe reduction in GFR (15-29 mL/min)
  • Stage 5: Kidney failure with GFR < 15 mL/min or dialysis


  • Blood Tests: Checking levels of creatinine and urea to estimate GFR.
  • Urine Tests: Assessing protein levels, which can indicate kidney damage.
  • Imaging Tests: Such as ultrasound to visualize kidney structure.
  • Kidney Biopsy: Sampling kidney tissue to determine the exact cause of kidney problems.


While CKD cannot typically be reversed, its progression can be slowed:

  • Control underlying conditions such as diabetes or hypertension.
  • Medications to lower blood pressure, reduce cholesterol, and treat anemia.
  • Adjust diet: reduce salt, protein, and potassium intake and manage fluid intake.
  • Avoid substances or medications toxic to the kidneys.
  • Dialysis or kidney transplantation in advanced stages.


  • Cardiovascular disease
  • High blood pressure
  • Anemia
  • Bone disease and abnormal calcium/phosphorus balance
  • Malnutrition
  • Nerve damage
  • Reduced immune response
  • Fluid overload


  • Regular medical check-ups to monitor blood pressure and blood sugar levels.
  • Healthy lifestyle: balanced diet, exercise, and weight control.
  • Limited use of medications that can harm the kidneys.
  • Monitoring and controlling conditions that can lead to CKD, like diabetes and hypertension.

Kidney Stones

Renal stones are solid, crystalline mineral accumulations originating in the kidneys. These formations exhibit a range of dimensions, spanning from minuscule grains of sand to substantial golf ball proportions. The level of discomfort associated with kidney stones is contingent upon their size and placement, ranging from painless to intensely agonizing, and in certain cases, they could obstruct the normal flow of urine.

Causes of Kidney Stones:

The formation of kidney stones can be attributed to several factors:

  • Saturation and Crystal Formation: Occurs when urine holds a surplus of crystal-forming elements (such as calcium, oxalate, and uric acid) that surpass the dilution capacity of the urine fluid.
  • Insufficient Urine Volume: Dehydration can lead to concentrated urine, promoting the crystallization of stone-forming minerals.
  • Urinary tract infections
  • Metabolic Disorders: Conditions that cause high excretion of certain substances in urine.
  • Certain Diets: High in protein, salt, or sugar.
  • Certain Medications: Such as calcium-based antacids, certain diuretics, and some antiseizure medications.

Varieties of Kidney Stones:

  • Calcium Stones: The most prevalent kind, frequently appearing as calcium oxalate formations. Elevated oxalate concentrations are present in select fruits, vegetables, nuts, as well as chocolate and tea.
  • Struvite Stones: Develop in response to infections, particularly urinary tract infections, and demonstrate rapid growth.
  • Uric Acid Stones: Commonly encountered in individuals with inadequate fluid intake, high-protein diets, or those afflicted by gout.
  • Cystine Stones: Emerge due to an inherited condition compelling the kidneys to expel excessive quantities of specific amino acids.

Symptoms of Kidney Stones:

Kidney stones often do not cause any symptoms when they remain in the kidneys. However, symptoms can emerge once a stone begins to move down the urinary tract or causes an obstruction.

The following are the common symptoms associated with kidney stones:

Severe Pain:

  • This is often the most telling sign. The location and intensity of the pain can change as the stone moves through the urinary tract.
  • Pain can begin sharp and severe in the back or side below the ribs and can radiate to the lower abdomen and groin.
  • The pain might come in waves and fluctuate in intensity.


  • Presence of blood in the urine, which can be visible (pink, red, or brown tinted urine) or microscopic (only detected through a lab test).

Cloudy or Foul-Smelling Urine:

  • Due to the presence of minerals or possibly a secondary infection.

Frequent Urination:

  • An increased urge to urinate, sometimes accompanied by a burning sensation when urinating.

Small Amounts of Urine:

  • Despite the frequent urge to urinate, only a small amount of urine is passed each time.

Nausea and Vomiting:

  • This can be due to the pain or because substances that promote stone formation have reached the intestine and caused an upset stomach.

Fever and Chills:

  • These symptoms are indicative of an infection in the urinary system, which is a complication that can arise from kidney stones.
  • Urine that appears cloudy or has an unpleasant smell: This might indicate an infection.


  • Blood Tests: To measure calcium, phosphorus, uric acid, and electrolytes.
  • Urine Tests: 24-hour urine collection test to check for minerals responsible for stone formation.
  • Imaging: X-rays, CT scans, or ultrasounds to visualize stones.


  • Small Stones: Drinking plenty of water to help pass the stone, pain relievers, and medical therapy to help pass the stone more easily.
  • Larger Stones and Those That Don't Pass: May require more invasive treatments like:
  • Extracorporeal Shock Wave Lithotripsy (ESWL): Uses sound waves to break the stone into smaller pieces.
  • Ureteroscopy: A thin tube is passed through the urinary tract to locate the stone, after which it can be broken up.
  • Percutaneous Nephrolithotomy: Surgery to remove a larger stone.
  • Parathyroid Gland Surgery: For stones caused by overactive parathyroid glands.


  • Drink plenty of water throughout the day.
  • Eat fewer oxalate-rich foods.
  • Choose a diet low in salt and animal protein.
  • Continue calcium intake, but be cautious with calcium supplements.


Glomerulonephritis (GN) is an inflammation of the glomeruli, which are tiny filtering units found within the kidneys. Each kidney has about a million glomeruli that help filter blood to produce urine. When these glomeruli are inflamed, the kidney's ability to filter waste, excess fluid, and electrolytes can be impaired.

Causes of Glomerulonephritis:

  • Immune Response: It can be a result of the body's immune response to an initial infection elsewhere, such as a throat infection or impetigo.
  • Autoimmune Diseases: Such as Lupus (SLE) or Goodpasture's syndrome, where the body's immune system attacks its own tissues.
  • Vasculitis: Inflammation of the blood vessels.
  • Certain Medications or Toxins.
  • Other kidney conditions, such as IgA nephropathy.
  • Unknown reasons (idiopathic).

Types of Glomerulonephritis:

  • Acute Post-streptococcal Glomerulonephritis: Occurs after a strep throat or skin infection.
  • Rapidly Progressive Glomerulonephritis: Kidney function deteriorates in days or weeks.
  • Membranous Glomerulonephritis: Due to thickening of the glomerular basement membrane.
  • Chronic Glomerulonephritis: Slow, progressive loss of kidney function over several years.
  • IgA Nephropathy: Caused by deposits of the protein IgA in the kidneys.

Symptoms of Glomerulonephritis:

  • Pink or dark-colored urine (due to red blood cells)
  • Foamy urine (due to excess protein)
  • High blood pressure
  • Fluid retention causing swelling in legs, ankles, and around the eyes
  • Fatigue or tiredness due to anemia or kidney failure
  • Frequent urination, especially at night


  • Blood Tests: To check levels of waste products like creatinine and urea.
  • Urine Tests: Detect blood, protein, and other signs indicating kidney damage.
  • Imaging Tests: Such as kidney ultrasound.
  • Kidney Biopsy: A definitive test where a small sample of kidney tissue is examined for signs of damage or inflammation.


The treatment for glomerulonephritis depends on its cause and type:

  • Blood Pressure Medications: To control hypertension and protect the kidneys.
  • Corticosteroids: To reduce inflammation.
  • Immunosuppressive Drugs: For cases caused by an overactive immune response.
  • Plasma Exchange: Used in some types of GN where blood plasma is removed and replaced with fluid or donor plasma.
  • Dietary Changes: Limiting protein, sodium, potassium, and phosphorus based on the level of kidney function.
  • Dialysis: In advanced stages or when kidney function deteriorates rapidly.


  • Acute kidney failure
  • Chronic kidney disease
  • High blood pressure
  • Nephrotic syndrome


While some forms of glomerulonephritis are hard to prevent:

  • Prompt treatment of throat and skin infections.
  • Regular medical check-ups, especially for those with risk factors.
  • Management of chronic conditions and avoidance of certain medications known to affect kidney function.

Polycystic Kidney Disease (PKD):

Polycystic Kidney Disease (PKD) is a hereditary condition marked by the development of multiple fluid-filled cysts within the kidneys. These cysts can lead to significant kidney enlargement, progressively diminishing their functionality. PKD may extend its influence to other organs like the liver. The disorder is classified into two main types: Autosomal Dominant PKD (ADPKD) and Autosomal Recessive PKD (ARPKD).

Causes of PKD:

  • ADPKD is usually inherited in an autosomal dominant manner, meaning only one copy of the abnormal gene (from either parent) is needed to develop the disease. It is primarily caused by mutations in the PKD1 or PKD2 genes.
  • ARPKD is a rarer form of the disease that is inherited in an autosomal recessive manner, meaning both copies of a gene (one from each parent) must be mutated for the disease to develop.

Symptoms of PKD:

Symptoms can vary and may include:

  • High blood pressure
  • Back or side pain
  • Blood in the urine
  • Kidney stones
  • Recurrent urinary tract infections
  • Abdominal pain or tenderness
  • Enlarged abdomen due to enlarged kidneys
  • Frequent urination
  • Liver and pancreatic cysts
  • Abnormal heart valves
  • Brain aneurysms


  • Family History: A detailed medical family history is critical as PKD is a genetic disorder.
  • Imaging Tests: Such as ultrasound, CT scans, or MRI to visualize cysts in the kidneys and other organs.
  • Genetic Testing: To identify mutations in PKD genes.
  • Blood Tests: To assess kidney function.


There is currently no cure for PKD, but treatment can manage symptoms and complications:

  • Blood Pressure Control: Managing blood pressure is a key aspect of PKD treatment. Common medications include ACE inhibitors and ARBs.
  • Pain Management: Over-the-counter pain medications or prescribed treatments.
  • Treatment of Infections: Prompt use of antibiotics to treat UTIs.
  • Diet and Lifestyle: A low-salt, low-fat diet, regular exercise, and quitting smoking can help manage blood pressure and slow the progression of kidney disease.
  • Surgery: To drain cysts that are causing pain or infections.
  • Tolvaptan: This is a newer medication that has been shown to slow the growth of cysts and the decline in kidney function in some people with ADPKD.
  • Dialysis or Kidney Transplant: For those who progress to end-stage renal disease (ESRD).


  • Chronic kidney disease (CKD), potentially leading to kidney failure
  • Liver cysts and other extrarenal (outside the kidney) cysts
  • Cardiovascular problems, including high blood pressure and heart valve abnormalities
  • Pregnancy complications, such as pre-eclampsia


As PKD is a genetic disorder, it cannot be prevented. However, people who are at risk due to family history may benefit from genetic counseling. Lifestyle modifications, such as a healthy diet, exercise, and blood pressure control, can help to manage symptoms and slow disease progression.

Make an appointment just in few minutes - Call Us Now