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PedAM

Pediatric Disease Annotations & Medicines




Disease n syndrome
Phenotype C0038238|steatorrhea
Sentences 4
PubMedID- 22104167 Background: anderson's disease (ad)/chylomicron retention disease (cmrd) is a rare hereditary hypocholesterolemic disorder characterized by a malabsorption syndrome with steatorrhea, failure to thrive and the absence of chylomicrons and apolipoprotein b48 post-prandially.
PubMedID- 26210192 Afferent loop syndrome should be suspected in case of malabsorption syndrome with chronic diarrhea, steatorrhea, iron-deficiency anemia, edema, emaciation, and osteomalacia and also in case of simple biological anomalies such as macrocytosis or megaloblastic anemia.
PubMedID- 22545223 The classic presentation of cd is a severe malabsorption syndrome with diarrhea, steatorrhea, and weight loss and possess antibodies against gliadin and especially tissue transglutaminase [2].
PubMedID- 23264789 [5] the classic presentation of severe malabsorption syndrome with chronic diarrhea, steatorrhea, and weight loss, however, is less common in cd that is known as the “iceberg” condition.

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