Health / Medical Topics

    Fanconi syndrome

    Pronunciation

    Definition 1

    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. Fanconi syndrome may also be caused by other diseases, a lack of vitamin D, or exposure to heavy metals or chemicals, including certain anticancer drugs. (NCI Dictionary)

    Definition 2

    A genetic or acquired disorder characterized by impairment of the function of the proximal tubules of the kidney. It results in decreased reabsorption of electrolytes, glucose, amino acids, and other nutrients. (NCI Thesaurus)




    YOU MAY ALSO LIKE

    Fanconi anemia-associated protein of 24 kDa (215 aa, ~24 kDa) is encoded by the human C19orf40 gene. This protein is involved in…
    Fanconi anemia-associated protein of 100 kDa (881 aa, ~93 kDa) is encoded by the human C17orf70 gene. This protein plays a role…
    Human fanconi anemia group M protein (2048 aa, ~23 kDa) is encoded by the FANCM gene. This nuclear ATPase is required for…
    Fanconi anemia group J protein (1249 aa, ~141 kDa) is encoded by the human BRIP1 gene. This protein is involved in DNA-dependent…
    Fanconi anemia group I protein (1328 aa, ~149 kDa) is encoded by the human FANCI gene. This protein plays a role in…
    Fanconi anemia group G protein (622 aa, ~69 kDa) is encoded by the human FANCG gene. This protein may be involved in…

    © 1991-2023 The Titi Tudorancea Bulletin | Titi Tudorancea® is a Registered Trademark | Terms of use and privacy policy
    Contact