abetalipoproteinemia
1Abetalipoproteinemia — Classification and external resources Micrograph showing enterocytes with a clear cytoplasm (due to lipid accumulation) characteristic of abetalipoproteinemia. Duodenal bi …
2abetalipoproteinemia — f. genét. Enfermedad hereditaria autosómica recesiva que provoca una mala absorción intestinal, ataxia, retinitis pigmentaria, anorexia, vómitos, diarrea, retraso del crecimiento y un aumento de peso del niño afectado. A los pocos años de edad… …
3Abetalipoproteinemia — Clasificación y recursos externos CIE 10 E78.6 CIE 9 272.5 OMIM …
4abetalipoproteinemia — Eng. Abetalipoproteinemia Ver acantocitosis …
5Abetalipoproteinemia — La Abetalipoproteinemia es una rara enfermedad que afecta al tracto digestivo, cuya principal característica es la incapacidad que tiene el organismo de absorber adecuadamente los componentes grasos del alimento a través del intestino, lo que… …
6abetalipoproteinemia — /ay bay teuh lip euh proh tee nee mee euh, tee euh nee , luy peuh , ay bee /, n. Pathol. a rare inherited disorder of fat metabolism due to an inability to synthesize betalipoproteins necessary for the transport of triglycerides, leading to… …
7abetalipoproteinemia — A disorder characterized by an absence of low density beta lipoprotein, presence of acanthocytes in blood, retinal pigmentary degeneration, malabsorption, engorgement of upper intestinal absorptive cells with dietary triglycerides, and …
8abetalipoproteinemia — noun a rare inherited disorder of fat metabolism; characterized by severe deficiency of beta lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels • Hypernyms: ↑hypobetalipoproteinemia, ↑lipidosis,… …
9normotriglyceridemic abetalipoproteinemia — a variant of abetalipoproteinemia in which apolipoprotein (apo) B 48 is present, but apo B 100 is absent; chylomicrons are formed but low density lipoproteins are not, and some fat absorption may occur …
10Bassen-Kornzweig syndrome — abetalipoproteinemia …
