Transport disease (recessive defect) in which the renal reabsorption of several substances (phosphate, glucose, amino acids) is impaired.
Fanconi syndrome (also known as Fanconi`s syndrome) is a disease of the proximal renal tubules of the kidney in which glucose, amino acids, uric acid, phosphate and bicarbonate are passed into the urine, instead of being reabsorbed. Fanconi syndrome affects the proximal tubule, which is the first part of the tubule to process fluid after it is fi....Found on http://en.wikipedia.org/wiki/Fanconi_syndrome
<syndrome> Transport disease (recessive defect) in which the renal reabsorption of several substances (phosphate, glucose, amino acids) is impaired. ... (18 Nov 1997) ... Found on http://www.encyclo.co.uk/local/20973
(fahn-ko´ne) Fanconi anemia; a rare autosomal recessive disorder characterized by pancytopenia, hypoplasia of bone marrow, and patchy brown discoloration of the skin due to deposition of melanin, with other anomalies of the musculoskeletal and genitourinary systems. any of a group of diseases marked by dysfuncti...Found on http://www.encyclo.co.uk/local/21001
Type: Term Pronunciation: fahn-kō′nē Definitions: 1. a type of idiopathic refractory anemia characterized by pancytopenia, hypoplasia of the bone marrow, and congenital anomalies, occurring in members of the same family (an autosomal recessive trait in at least five nonallelic types [MIM*227650, 227600, 227645, 227646, 600901]); the...Found on http://www.medilexicon.com/medicaldictionary.php?t=87964
A group of kidney disorders that cause protein, sugar, minerals, and other nutrients to be lost in the urine. Symptoms include weakness, bone pain, and passing a greater than normal amount of urine. One form of Fanconi syndrome is inherited and is usually found in infants. FanconiFound on http://www.cancer.gov/dictionary?expand=F
No exact match found