Rare diseases are in a special global classification and information about them is updated by all countries in the world. In many cases, their symptoms are difficult to detect because they require specialized tests or information from the patient or his relatives about heredity. Unfortunately, some of them have a negative prognosis or require long-term treatment and continuous monthly follow-up. A rare disease is considered to be one that affects 1 in 2000 people, with 6-7000 types identified to date and unfortunately the list is growing. Some of these rare diseases are:
- neuromuscular diseases;
- neurofibromatosis;
- cystic fibrosis;
- chondrodysplasia (Rett syndrome);
- amyotrophic lateral sclerosis;
- Kaposi's sarcoma and many more.
We can help you with highly skilled medical assistance from specialist medical teams, experienced and skilled in this difficult and problematic area.
Learn more about diseases:
Wolff-Hirschhorn syndrome also known as 4p-syndrome
Osteogenesis imperfecta - the glass bones
Progeria or Hutchinson-Gilford syndrome
