The following Conditions are related to Gl

Select a specific condition below to view its details.

  • Crosti-gianotti syndrome

    Gianotti-Crosti syndrome (GCS), papular acrodermatitis of childhood or acrodermatitis is a rare, childhood skin condition that affects children between the ages of 3 months and 15 years.Gianotti-Crosti syndrome is characterized by a papular rash with blisters on the skin of the legs, buttocks, and arms.Skin lesions typically last at least 10 days but may last for several weeks. GCS is a response to the und  Read More

  • Ectodermal dysplasias

    Each of the nearly 100 EDs has its own set of clinical signs and symptoms. Commonly, the conditions will have one or more of the following associated findings: Teeth: reduced number, abnormal shape or size Hair: abnormal structure, sparse, slow-growing, often light-colored Sweat glands: often reduced number and abnormal structure, leading to decreased sweat production and risk of elevated body temperature (hy  Read More

  • Gangrene

    Damaged tissue from gangrene cannot be saved. However, medication is available to help avoid gangrene from worsening. The sooner you receive therapy, the greater your chances of recovery.Gangrene treatment may comprise one or more of the following: Medication: Antibiotics are administered intravenously or orally to treat bacterial infections. To alleviate discomfort, pain medicines may be admini  Read More

  • Hives, giant

    Angioedema or Hives is usually treated by avoiding known triggers to the allergic reaction.The prescription drugs for the treatments of hives and angioedema may include:Antihistamines: It is the standard treatment for hives and angioedema. These medications reduce itching, swelling and other allergy symptoms.Drugs that suppress the immune system: Drugs that can calm an overactive immune system  Read More

  • Localized epidermolysis bullosa

    Localized Epidermolysis bullosa simplex (EBS) is a genetic disease, which means that it is caused by one or more genes not working correctly.The majority of EBS subtypes are inherited in a dominant manner. This means that an affected parent passes them on to half of his or her offspring. EBS affects both men and women equally.Epidermolysis bullosa simplex is often transmitted in an autosomal dominant manne  Read More

  • Morgagni-stewart-morel syndrome

    Morgagni-Stewart-Morel syndrome is in-short, known as MSM syndrome.The exact cause of the disease is yet to be unraveled, and its manifestations are yet to be completely described.The disease was known to cause neurological manifestations.However, endocrinal and metabolic abnormalities have been found to be associated with the disease.The autosomal dominant genetic mutations have been bel  Read More

  • Panniculitis, idiopathic nodular

    Idiopathic nodular panniculitis is a rare spectrum of skin disorders characterized by single or multiple, tender or painful bumps below the surface of the skin subcutaneous nodules) that can be open sores and usually lead to inflammation of the subcutaneous layer of fat (panniculitis).These nodules tend to be 1-2 centimeters in size and most often affect the legs and feet Rare cases involve panniculitis of the brea  Read More

  • Rapp hodgkin syndrome

    Rapp-Hodgkin syndrome is a rare disease that is caused by a defect in genes. It can cause problems to hair, nails, skin, teeth, and sweat glands. The child may inherit one faulty gene from each parent and resulting in this syndrome.The child with Rapp-Hodgkin syndrome may have opened in the upper lip, skin erosions, fused eyelids, growth problems, hair loss, and other problems associated with appearance. him99999 U  Read More

  • Van lohuizen syndrome

    An uncommon congenital skin condition known as Van Lohuizen Syndrome, is marked by discoloured patches of skin (livedo reticularis) brought on by dilated surface blood vessels (telangiectases), which give the skin a ""fishnet"" or blue or purple appearance. This condition is commonly accompanied by skin sores (Ulcers) that resemble craters. At least 50% of those with the condition also have other congenital  Read More