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Microvillus inclusion disease, also known as Davidson's disease, congenital microvillus atrophy and, less specifically, microvillus atrophy (note: microvillus is often misspelled as microvillous), is a rare genetic disorder of the small intestine that is inherited in an autosomal recessive pattern.〔 〕〔Mills SE, Carter D, Greenson JK, Oberman HA, Reuter V, Stoler MH. Sternberg's Diagnostic Surgical Pathology. 4th Ed. Lippincott Williams & Wilkins. Copyright 2004. ISBN 978-0-7817-4051-7.〕 ==Presentation== It is characterized by chronic, intractable diarrhea in new-born infants, starting in the first few days of life.〔 〕 This results in metabolic acidosis and severe dehydration. Pregnancy and birth are usually normal. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「microvillous inclusion disease」の詳細全文を読む スポンサード リンク
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