Mucopolysaccharidosis
| Description | Mucopolysaccharid evaluation in the urine. Molecular-genetic evaluation possible for type I (Hurler syndrome), type II (Hunter’s syndrome), type IIIA (Sanfilippo A syndrome), type IIIB (Sanfilippo B syndrome), type IVA (Morquio A syndrome) |
More Results for the letter M
- Macrosomia
- Malabsorption
- MALT-syndrome (Mucosa associated lymphoid tissue lymphoma)
- Malta fever, familial
- Mamma-carcinoma
- Maple sirup urine disease, MSUD
- Marchiafava-Micheli-syndrome
- Marfan-syndrome
- Mastitis
- Mastocytosis
- Mastodynia/mastalgia
- Maternity screening
- MCTD
- Medullary thyroid carcinoma (C-cell carcinoma)
- Melanoma
- Membrane-proliferative glomerulonephritis type II
- MEN 1 and 2
- Meningitis
- Menopause
- Menopause
- Mental retardation
- Mercury poisoning
- Metabolic disorders, congenital
- Metabolic syndrome
- Metachromatic leukodystrophy
- Metrorrhagia
- Microhematuria
- Microscopic polyarteritis
- Microsomia
- Migraine