Grayson’s Syndrome
Grayson's Syndrome is a mitochondrial disorder that is highly uncommon. This illness, also known as Grayson Wilbrandt corneal dystrophy (GWCD), is one of the most uncommon kinds of corneal dystrophy,…
Grayson's Syndrome is a mitochondrial disorder that is highly uncommon. This illness, also known as Grayson Wilbrandt corneal dystrophy (GWCD), is one of the most uncommon kinds of corneal dystrophy,…
Overview The median arcuate ligament syndrome, MALS (also known as celiac artery compression syndrome) is a rare disorder characterized by postprandial stomach discomfort, accidental weight loss, and an epigastric bruit.…
Overview The Klippel Trenaunay syndrome is an uncommon congenital disorder characterized by abnormal formation of blood vessels and/or lymph vessels. The syndrome is characterized by three features: a port-wine stain,…
Overview Olmsted syndrome is an uncommon congenital palmoplantar keratoderma that is finely circumscribed and progressive. These lesions are accompanied by reddish skin and joint deformities that cause restriction and spontaneous…
Overview of purple urine bag syndrome Purple urine bag syndrome (PUBS) is a complication of urinary tract infections (UTIs) characterized by the discoloration of catheter bags and tubing. It is…
Overview of Eczema ‘Eczema’ is a very commonly known skin condition. It is a Greek word. The meaning of eczema is ‘to boil’. Many people use the word eczema to…
Overview of Menkes disease A faulty ATP7A gene causes Menkes disease, a hereditary genetic disorder. Menkes syndrome causes copper absorption deficiency. This results in arterial changes and degeneration of the…
XXYY syndrome is a chromosomal disorder defined by the presence of an extra X and Y chromosome in men and is associated with medical and behavioral issues. XXYY is a…
Overview Brittle bone disorder results in bones that are weak and shatter readily. It typically manifests at birth, however it has only been documented in children with a family history…
Overview of Huntington's disease Huntington's disease is an inherited condition. It is transmitted from parents to offspring. If a parent has Huntington's disease, there is a 50% risk that the…
Osteoporosis is a condition characterized by the degeneration and weakness of bone tissue. Over time, osteoporosis might progress. This can lead the bone to become progressively porous and more brittle…
Overview Juvenile idiopathic arthritis (formerly known as systemic juvenile rheumatoid arthritis) is an umbrella term encompassing adolescent rheumatic disorders that begin before the age of 16 and are defined by…
Treacher-Collins syndrome is also known as Lancaster disease or Franceschetti-Zwahlen-Klein syndrome. It is a rare genetic disorder manifested by the head's bony and soft tissue deformities, especially ears, orbit, facial…
Peritoneal mesothelioma is a malignancy that develops in the peritoneum, which is the lining of the abdomen. The most effective treatment for this kind of mesothelioma is surgery with hot…
Silica exists naturally in the majority of rocks, sand, and clay, as well as in products such as bricks and concrete. Additionally, silica is utilized as a filler in some…