GIST tumor GIST tumor is short for gastrointestinal stromal tumor, is a rare type of tumor that occurs in the gastrointestinal tract, most commonly in

Osteonecrosis hip Osteonecrosis of the hip also called osteonecrosis of the femoral head, aseptic necrosis of the femoral head or avascular necrosis, is a condition where

Lomatium Lomatium also known as biscuitroot, Indian parsley, or desert parsley belongs to a family of mostly aromatic flowering plants called Apiaceae (carrot family) ((Setzer WN, Poudel

What is methylene blue Methylene blue (C16H18ClN3S), also known as methylthioninium chloride or tetramethylthionine chloride, is a medication and an oxidation-reduction agent that is used to treat

What is MCT oil MCT oil is short for medium chain triglyceride oil or medium-chain triacylglycerol or saturated fatty acid with carbon chain lengths ranging from C6,

Anti-inflammatory foods When your body is in an inflammatory state that can trigger pain and cause diseases, what you eat may increase inflammation and set

Red light therapy Red light therapy also known as non-thermal LED light, low-intensity long-wavelength red light, low-level red light therapy, low-power laser therapy, low-level laser therapy (LLLT) or cold laser therapy

Mycosis fungoides Mycosis fungoides is the most common form of cutaneous T cell lymphoma or non-Hodgkin lymphoma that first appears on the skin and can spread to

Ozempic Ozempic is a brand name for a weekly subcutaneous injection medicine called Semaglutide that is used together with diet and exercise to treat type 2 diabetes in

ALA dehydratase deficiency porphyria ALA dehydratase deficiency porphyria (ADP) also called ALAD deficiency porphyria, delta-aminolevulinate dehydratase deficiency or Doss porphyria is an extremely rare genetic disorder that involve defects

Variegate porphyria Variegate porphyria (VP) also known as South African genetic porphyria is a rare genetic disorder that involve defects in heme or ‘haem’ biosynthetic pathway caused by mutations

Hereditary coproporphyria Hereditary coproporphyria (HCP) is a rare inherited form of liver (hepatic) porphyria, that involve defects in heme or ‘haem’ biosynthetic pathway caused by