Traduction de «histochemical lipidosis » (Anglais → Français) :

histochemical lipidosis
lipidose histochimique

histochemical technique
technique histochimique

immuno-histochemical technique
technique immuno-histochimique

metachromatic leukodystrophy [ MLD | sulfatide lipidosis ]
leucodystrophie métachromatique [ spihingolipidose à sulfatide | maladie de Scholz ]

lipidosis
lipidose [ dyslipidose | dyslipoïdose ]

Disease that is characterized by massive enteric protein loss, secretory diarrhea and intolerance to enteral feeds during the first few weeks of life. It has been described in three male infants. Histochemical studies revealed a complete absence of e
déficit congénital en héparane sulfate de l'entérocyte

DAF syndrome | lipid histiocytosis | lipoid histiocytosis (classical phosphatide) | Niemann-Pick disease | sphingomyelin lipidosis | sphingomyelinase deficiency
histiocytose lipoïdique essentielle | maladie de Niemann-Pick | sphingomyélinose

Dementia in:cerebral lipidosis (E75.-+) | epilepsy (G40.-+) | hepatolenticular degeneration (E83.0+) | hypercalcaemia (E83.5+) | hypothyroidism, acquired (E01.-+, E03.-+) | intoxications (T36-T65+) | multiple sclerosis (G35+) | neurosyphilis (A52.1+) | niacin deficiency [pellagra] (E52+) | polyarteritis nodosa (M30.0+) | systemic lupus erythematosus (M32.-+) | trypanosomiasis (B56.-+, B57.-+) | vitamin B12 deficiency (E53.8+)
Démence au cours de:carence en:acide nicotinique [pellagre] (E52+) | vitamine B12 (E53.8+) | dégénérescence hépatolenticulaire (E83.0+) | épilepsie (G40.-+) | hypercalcémie (E83.5+) | hypothyroïdie acquise (E01.-+, E03.-+) | intoxications (T36-T65+) | lipidose cérébrale (E75.-+) | lupus érythémateux disséminé (M32.-+) | neurosyphilis (A52.1+) | périartérite noueuse (M30.0+) | sclérose en plaques (G35+) | trypanosomiase (B56.-+, B57.-+)

Sulfatide lipidosis
leucodystrophie métachromatique

Cerebral lipidosis
lipidose cérébrale