Enciclopedia Universal. 2012.
Abetalipoproteinemia — Classification and external resources Micrograph showing enterocytes with a clear cytoplasm (due to lipid accumulation) characteristic of abetalipoproteinemia. Duodenal bi … Wikipedia
abetalipoproteinemia — 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… … Diccionario médico
Abetalipoproteinemia — Clasificación y recursos externos CIE 10 E78.6 CIE 9 272.5 OMIM … Wikipedia Español
abetalipoproteinemia — Eng. Abetalipoproteinemia Ver acantocitosis … Diccionario de oftalmología
abetalipoproteinemia — /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… … Universalium
abetalipoproteinemia — 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 … Medical dictionary
abetalipoproteinemia — 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,… … Useful english dictionary
normotriglyceridemic 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 … Medical dictionary
Bassen-Kornzweig syndrome — abetalipoproteinemia … Medical dictionary
Microsomal triglyceride transfer protein — Identifiers Symbols MTTP; ABL; MGC149819; MGC149820; MTP External IDs … Wikipedia
