Malta fever, familial
Description | Clinical presentation: Recurrent high fever with peritoneal, arthritic or pleuritic symptoms in patients from the Mediterranean. Frequency of the homozygote type 1:2000. Molecular-genetic evaluation possible. Please also refer to section “Malta fever” (analysis index)
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More Results for the letter M
- Miller-Fisher-syndrome
- Missed abortion
- MOGAD (MOG-Antibodies-associated disease)
- Monoclonal gammopathy
- Monocytosis (> 800 µl)
- Morbus hemolyticus neonatorum / Hemolytic disease of the newborn
- Movement disorders
- Mucopolysaccharidosis
- Mucoviscidosis
- Multiple chemical sensitivity (MCS)
- Multiple endocrine neoplasia type 1 (MEN 1)
- Multiple endocrine neoplasia type 2A and 2B (MEN 2A and MEN 2B)
- Multiple myeloma (plasmocytoma) and Waldenstöm’s disease
- Multiple Sclerosis
- Muscle atrophy, spinal and spinobulbar
- Muscle dystrophy type Becker (BMD) and Duchenne (DMD)
- Muscle spasms /cramps
- Muscle weakness / myasthenia
- Myalgia
- Myasthenia gravis
- Mycosis fungoides
- Myelitis
- Myelodysplastic syndrome (MDS)
- Myocardial infarction
- Myocarditis
- Myopathy (degenerative myopathy)
- Myositis (inflammatory myopathy)