Fanconi syndrome laboratory findings: Difference between revisions

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{{Fanconi syndrome}}
{{Fanconi syndrome}}
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{{CMG}}; {{AE}} {{VE}}
 
==Overview==
==Overview==
Urinary lab tests are more diagnostic than plasma because of more prominent findings.
Plasma and urinary lab tests in Fanconi syndrome indicate on the expected alterations in the concentration of electrolytes, metabolites and nutrients in concordance to unregulated urinary excretion. Urinary lab tests are more diagnostic than plasma because of more prominent findings.


==Laboratory Findings==
==Laboratory Findings==
Labratory findings are not consistent in every case of Fanconi syndrome and the severity extent of each findings varies case by case mostly depended on the underlying etiology. Many of these findings are common with [[Proximal renal tubular acidosis]]<ref name="pmid23235953">{{cite journal| author=Haque SK, Ariceta G, Batlle D| title=Proximal renal tubular acidosis: a not so rare disorder of multiple etiologies. | journal=Nephrol Dial Transplant | year= 2012 | volume= 27 | issue= 12 | pages= 4273-87 | pmid=23235953 | doi=10.1093/ndt/gfs493 | pmc=3616759 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23235953  }}</ref><ref>Enriko Klootwijk, Stephanie Dufek, Naomi Issler, Detlef Bockenhauer & Robert Kleta (2016)Pathophysiology, current treatments and future targets in hereditary forms of renal Fanconi syndrome,Expert Opinion on Orphan Drugs, 5:1, 45-54, DOI: 10.1080/21678707.2017.1259560</ref><ref name="pmid13381735">{{cite journal| author=ENGLE RL, WALLIS LA| title=The adult Fanconi syndrome.  II.  Review of eighteen cases. | journal=Am J Med | year= 1957 | volume= 22 | issue= 1 | pages= 13-23 | pmid=13381735 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=13381735  }}</ref>.
* [[Hypophosphatemia]]/Phosphaturia
* [[Hypophosphatemia]]/Phosphaturia
* [[Glycosuria]] with normal plasma glucose levels (rarely leads to hypoglycemia)
* [[Glycosuria]] with normal plasma glucose levels (rarely leads to [[hypoglycemia]])
* [[Proteinuria]]/Aminoaciduria
* [[Proteinuria]]/[[Aminoaciduria]]
* [[Uricosuria]]/Hypouricemia
* [[Uricosuria]]/[[Hypouricemia]]
* Natriuresis/Hyponatremia
* Natriuresis/[[Hyponatremia]]
* Kaliuria/Hypokalemia
* Kaliuria/[[Hypokalemia]]
* Low anion gap Metabolic acidosis (from bicarbonate loss)
* Low [[anion gap]] [[Metabolic acidosis]] (from bicarbonate loss)
* Hypovolemia from glucose osmotic diuresis and renal sodium loss
* [[Hypovolemia]] from glucose osmotic [[diuresis]] and renal sodium loss


==References==
==References==

Latest revision as of 16:34, 21 July 2018

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vahid Eidkhani, M.D.

Overview

Plasma and urinary lab tests in Fanconi syndrome indicate on the expected alterations in the concentration of electrolytes, metabolites and nutrients in concordance to unregulated urinary excretion. Urinary lab tests are more diagnostic than plasma because of more prominent findings.

Laboratory Findings

Labratory findings are not consistent in every case of Fanconi syndrome and the severity extent of each findings varies case by case mostly depended on the underlying etiology. Many of these findings are common with Proximal renal tubular acidosis[1][2][3].

References

  1. Haque SK, Ariceta G, Batlle D (2012). "Proximal renal tubular acidosis: a not so rare disorder of multiple etiologies". Nephrol Dial Transplant. 27 (12): 4273–87. doi:10.1093/ndt/gfs493. PMC 3616759. PMID 23235953.
  2. Enriko Klootwijk, Stephanie Dufek, Naomi Issler, Detlef Bockenhauer & Robert Kleta (2016)Pathophysiology, current treatments and future targets in hereditary forms of renal Fanconi syndrome,Expert Opinion on Orphan Drugs, 5:1, 45-54, DOI: 10.1080/21678707.2017.1259560
  3. ENGLE RL, WALLIS LA (1957). "The adult Fanconi syndrome. II. Review of eighteen cases". Am J Med. 22 (1): 13–23. PMID 13381735.