Mediterranean fever, familial
| Material: | 1 ml – 2 ml EDTA-blood and declaration of consent |
| Clinical presentation | The familial Mediterranean fever is a genetic disease with recurrent fever spells and acute peritonitis, often pleuritic or arthritis (sacroiliitis) and development of amyloidosis with subsequent renal insufficiency. Frequent occurrence already in childhood. The significance of a molecular genetic diagnosis of this not uncommon disease lies in the opportunity of an effective amyloidosis prophylaxis with colchicine. |
| External services | ja MVZ Dr. Eberhard & Partner Dortmund |
More Results for the letter M
- Macro enzymes (MAKROENZ)
- Macro prolactin (MAKRO)
- Macro-CK (CKM1)
- Macroamylase (AMYMA)
- Macroprolactin (MPROL)
- Magnesium (Mg) in serum (MG)
- Magnesium (Mg) in urine (MGU)
- Malaria (IMALA)
- Plasmodia
- Malondialdehyde (MALDI)
- MDA
- Manganese (Mn) in blood and urine (MANGE)
- Maprotiline (MAP)
- Maternity screening (MUVO)
- Measles (MASE)
- Group of the paramyxoviruses, serotype 1
- Medical drugs, therapeutic ranges and toxic levels (MDRUG)
- Mediterranean fever, familial (MEFV)
- Melanin/Melanogen (MELA)
- Melatonin (MELAT)
- Mercury in blood, urine and saliva (MERC)
- Metals in plasma (MEA)
- Multi-element analysis
- Metals in urine (MEAU)
- Multi-element analysis (MEA)
- Metanephrine, normetanephrine in plasma (METAPL)
- Metanephrine, normetanephrine in urine (METAU)
- Methadon (METHU)
- Methanol (METHAB)
- Methyl alcohol
- Methemoglobin (METHB)
- Met-Hb
- Methotrexate (METHO)
- MTX
- Methsuximide (MESUD)
- N-desmethyl-methsuximide
- Methyl hippuric acid, total (MHIP)
- Ortho-, meta,- para-methyl hippuric acid
- Methyl histamine (METHYL)
- 1,4-methylimidazole acetic acid, metabolite of histamine in the urine
- Methylhippuric acid, total (METH04)
- ortho-, meta-, para-methylhippuric acid