Bartter disease type 3 is a rare, inherited kidney condition. The kidneys normally reabsorb salt (sodium chloride) from the urine back into the blood. In type ...
Dr. Huma Q. Rana, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist
Infantile polycystic kidney disease—usually called autosomal recessive polycystic kidney disease (ARPKD)—is a genetic disease. A baby is born with it when they ...
Dr. Reem Saadeh Haddad, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist
Introduction Gallbladder cancer is a rare but serious disease that develops when cancerous (malignant) cells form in the tissues of the gallbladder a small ...
Dr Muhammad Zakria
Introduction Liver cancer is one of the most challenging cancers worldwide, known for its aggressive nature and often late diagnosis. ...
Sarcotubular myopathy is a rare, inherited muscle disease. It usually runs in families in an autosomal recessive way and is most often caused by harmful ...
Autosomal recessive distal renal tubular acidosis is a rare, inherited kidney condition. It affects the last part of the kidney tubule called the distal ...
Kidney tubular acidosis is a group of disorders where the kidney’s tubules can’t keep the body’s acid-base balance normal. You get a normal anion-gap ...
Autosomal dominant Alport syndrome (ADAS) is a genetic kidney condition caused by a single (heterozygous) disease-causing change in one copy of the COL4A3 or ...
Goodpasture syndrome—also called anti-glomerular basement membrane (anti-GBM) disease—is a rare, fast-moving autoimmune disease. The immune system makes ...
Dr. Priya Kishnani, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist
Anti-Glomerular Basement Membrane (anti-GBM) Disease is a rare autoimmune illness. Your immune system makes harmful antibodies that mistakenly attack a ...
Creatine deficiency syndrome is a group of rare, inherited brain energy disorders. In these conditions, the brain cannot make, move, or bring in enough ...
Dr. Nadia Falah, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist
Nephronophthisis is an inherited kidney disease where the tiny tubules (pipes) inside the kidney slowly scar and form small cysts near the border between the ...
Tubulointerstitial nephritis (TIN) is inflammation and injury that mainly affect the tubules (the tiny pipes that balance water, salt, acid–base, and waste) ...
Dr. Kira Manusis MD - Ophthalmologist
Urinary Dysbiosis refers to an imbalance in the naturally occurring microorganisms (the microbiome) within the urinary tract. For many years, urine was thought ...
Dr. Azin Abazari, MD - Ophthalmologist
Uvula muscle tendinitis is a condition in which the small muscle of the uvula (the soft, hanging tissue at the back of your throat) becomes inflamed or ...
Dr. Nicole L. Aaronson MD -Otolaryngology (ENT)
Piriformis fascia adhesions are a condition involving abnormal fibrous bands that form in the fascia surrounding the piriformis muscle. These adhesions can ...
Sarmela Sunder
Piriformis fascia hyperplasia is a condition that affects the piriformis muscle and its fascia—a layer of connective tissue that covers the muscle. In this ...
Piriformis fascia fibrosis is a condition where the connective tissue (fascia) around the piriformis muscle becomes thickened or scarred. This fibrosis can ...
Piriformis fascia fibrosis is a condition where the connective tissue (fascia) around the piriformis muscle becomes thickened or scarred. This fibrosis can ...
Piriformis fascia cysts are fluid-filled sacs that can develop in or around the fascia (the connective tissue) that covers the piriformis muscle in the buttock ...
