Metabolic disorders, congenital
| Description | (Organ acidurias, aminoacidopathies and others) Basic evaluations: Blood: Full blood count, electrolytes (anion deficit), glucose, creatinine, urea, uric acid, CK, cholesterol, triglycerides, GOT, GPT, gamma-GT, PTT, INR, ammoniac, lactate, pyruvate, hydroxybutyrate Urine: Ketone bodies, reducing substances (Clinitest), sulfite test in fresh urine (sulfite oxidase deficiency), urea, creatinine Selective screening: Screening for congenital metabolic disorders
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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