rare diseases

In imprisonment syndrome the person gets stuck in his own body and is unable to move, despite being awake. Understand.

For the treatment of amyloidosis, the doctor may indicate the use of medication, radiotherapy, use of stem cells, surgery or transplantation.

Weaver's syndrome is a rare childhood condition that causes overgrowth and lack of strength, as well as wide eyes and a large forehead.

Caroli syndrome is a rare disease that affects the liver causing constant abdominal pain. This disease has no cure and treatment may include medication, surgery and even liver transplantation.

What it is: Epispadia is a rare defect of the genitals, which can appear in both boys and girls, being identified early in childhood. This change causes the opening of the urethra, the channel that carries urine from the bladder out of the body, n

Vincent's angina, also known as acute necrotizing ulcerative gingivitis, is a rare and severe disease of the gums. See what it consists of, what are the most common causes and symptoms and how is the treatment done

Sclerosing cholangitis is a rare disease in which there is obstruction of the channel through which bile passes, which can lead to the appearance of some symptoms such as yellow skin and eyes and muscle weakness. Understand what is sclerosing cholangitis, what are the symptoms

Antiphospholipid Antibody Syndrome is a rare autoimmune disease characterized by the ease of forming thrombi in veins and arteries, which can cause serious complications. See what is at the origin of this disease and what treatment options are available

Vogt-Koyanagi-Harada Syndrome is a rare disease that affects tissues that contain melanocytes, such as the eyes, central nervous system, ear and skin. See the symptoms of this disease and what the treatment consists of.

Fanconi syndrome is a rare disease of the kidneys that causes the exaggerated elimination of various substances in the urine, resulting in symptoms such as strong-smelling urine, excessive thirst and even developmental problems. Understand better what the syndrome is

Parry-Romberg syndrome, or just Romberg syndrome, is a rare disease that is characterized by atrophy of the skin, muscle, fat, bone tissue and nerves of the face, causing aesthetic deformation. Generally, this disease only affects one side of the face