rare diseases

Scheuermann's disease is a rare disease that causes a deformity of the curvature of the spine, producing arching of the back and pain. See other symptoms, how is the diagnosis and how should the treatment be

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.

Holt-Oram Syndrome is a rare genetic disease that causes deformities in the upper limbs, such as hands and shoulders and heart problems. Know more.

Crouzon syndrome, also known as craniofacial dysostosis, is a rare disease that leads to several cranial and facial deformities in the baby. Better understand why it happens, what the symptoms are and how the treatment can be done

Chimerism is a rare genetic alteration in which the presence of two or more populations of cells with different genetic characteristics is verified. Understand what chimerism is, what types and how to identify

What it is: Swyer syndrome, or pure gonadal dysgenesis XY, is a rare disease where a woman has male chromosomes and that is why her sex glands do not develop and she does not have a very feminine image. Its treatment is done with the

Bubonic plague is a serious disease caused by the bacterium Yersinia pestis. Infection with this bacterium is treated with the administration of antibiotics and preventive measures to control rodents and pests. Learn more about treating Yersinia infection

Idiopathic thrombocytopenic purpura is an autoimmune disease in which the body's own antibodies destroy blood platelets. See what are the main symptoms and how the treatment is done

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

Wilson's disease is a genetic disease characterized by the accumulation of copper in the body, mainly the brain, kidneys and liver. Understand what Wilson's disease is, symptoms, treatment and how the diagnosis is made.

Paroxysmal nocturnal hemoglobinuria is a rare genetic disease characterized by the destruction of red blood cells, leading to symptoms such as weakness, drowsiness and abdominal pain. Learn more about this disease and how the diagnosis is made.

The treatment for generalized congenital lipodystrophy, which is a genetic disease that does not allow the accumulation of fat under the skin leading to its accumulation in organs or muscles, aims to reduce the symptoms and, therefore, varies in each case. Per

Treatment for Zollinger-Ellison syndrome is usually started with the daily intake of drugs to reduce the amount of acid in the stomach, such as Omeprazole, Esomeprazole or Pantoprazole, as tumors in the pancreas, called gastrinomas

Red man syndrome is a situation that can occur immediately or after a few days of using the antibiotic vancomycin due to a hypersensitivity reaction to this drug. This medicine can be used for the treatment of orthopedic diseases

Haff's disease is a rare condition that causes black urine to appear and other symptoms such as muscle pain, numbness and loss of strength. Generally, the disease is caused by the ingestion of a toxin present in freshwater fish. Understand better

Fibrodysplasia ossificans progressiva (FOP) is a rare disease that causes the muscles to turn into bone, preventing the person from moving. Better understand what causes this condition, what the symptoms are and how the treatment is done

Hermaphroditism is a genetic condition in which a person is born with two genitals, both male and female. Although there are 3 types of hermaphrodite, only one is considered true. Better understand the condition, its types and see

Amyloidosis is a disease characterized by the accumulation of proteins in the body, affecting organs such as the heart, lung, kidneys and brain. See the types and symptoms.

Gartner's cyst is a type of vaginal lump that can cause symptoms such as pain during intimate contact and discomfort in the region. Understand why it appears, what are the associated symptoms and how the treatment is done

Pigeon breast is the popular name given to a rare malformation, known scientifically as Pectus carinatum, in which the sternum bone is more detached, causing a protrusion in the chest. See what causes this change and what treatment options to fix