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{{Infobox disease |
{{Infobox medical condition (new)
Name = Xanthinuria |
| name =
ICD10 = {{ICD10|E|79|8|e|70}} |
| image = Xanthin - Xanthine.svg
ICD9 = {{ICD9|277.2}} |
| caption = [[Xanthine]]
ICDO = |
| pronounce =
Image = Xanthin - Xanthine.svg |
| field =
Caption = [[Xanthine]] |
| synonyms =
OMIM = 278300 |
| symptoms =
| complications =
⚫
OMIM_mult = {{OMIM2|603592}} |
MedlinePlus = |
| onset =
| duration =
⚫
eMedicineSubj = ped |
| types =
⚫
eMedicineTopic = 2452 |
DiseasesDB = 14194 |
| causes =
| risks =
DiseasesDB_mult = {{DiseasesDB2|29821}} |
MeshName = |
| diagnosis =
MeshNumber = |
| differential =
| prevention =
| treatment =
| medication =
| prognosis =
| frequency =
| deaths =
}}
}}


'''Xanthinuria''', also known as '''xanthine oxidase deficiency''', is a rare [[genetic disorder]] causing the accumulation of [[xanthine]]. It is caused by a deficiency of the [[enzyme]] [[xanthine oxidase]].
'''Xanthinuria''', also known as '''xanthine oxidase deficiency''', is a rare [[genetic disorder]] causing the accumulation of [[xanthine]]. It is caused by a deficiency of the [[enzyme]] [[xanthine oxidase]].


It was first formally characterized in 1954.<ref>{{cite journal
It was first formally characterized in 1954.<ref>{{cite journal|vauthors=Dent CE, Philpot GR | title = Xanthinuria, an inborn error (or deviation) of metabolism| journal = [[The Lancet|Lancet]]| year = 1954| volume = 266| issue = 6804| pages= 182–5 |pmid=13118765 | doi =10.1016/S0140-6736(54)91257-X }}</ref>

| author = Dent CE, Philpot GR
⚫
==Presentation==
| title = Xanthinuria, an inborn error (or deviation) of metabolism
⚫
Affected people have unusually high concentrations of xanthine in their blood and urine, which can lead to health problems such as [[renal failure]] and xanthine kidney stones, one of the rarest types of kidney stones.{{cn|date=October 2024}}
| journal = [[The Lancet|Lancet]]
| year = 1954
| volume = 266
| issue = 6804
| pages= 182–5 |pmid=13118765
| doi =10.1016/S0140-6736(54)91257-X }}</ref>


==Causes==
==Causes==
It can be caused by a deficiency of [[xanthine oxidase]], which is an enzyme necessary for converting [[xanthine]] to [[uric acid]].<ref name="pmid9153281">{{cite journal |author=Ichida K, Amaya Y, Kamatani N, Nishino T, Hosoya T, Sakai O |title=Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria |journal=[[J. Clin. Invest.]] |volume=99 |issue=10 |pages=2391–7 |year=1997 |pmid=9153281 |pmc=508078 |doi=10.1172/JCI119421}}</ref>
Type I xanthinuria can be caused by a deficiency of [[xanthine oxidase]], which is an enzyme necessary for converting [[xanthine]] to [[uric acid]].<ref name="pmid9153281">{{cite journal |vauthors=Ichida K, Amaya Y, Kamatani N, Nishino T, Hosoya T, Sakai O |title=Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria |journal=[[J. Clin. Invest.]] |volume=99 |issue=10 |pages=2391–7 |year=1997 |pmid=9153281 |pmc=508078 |doi=10.1172/JCI119421}}</ref> Type II xanthinuria and [[molybdenum cofactor deficiency]] lack one or two other enzyme activities in addition to xanthine oxidase.<ref>{{cite journal | author = Ichida K, Amaya Y, Kamatani N, Nishino T, Hosoya T, Sakai O | title = Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria | journal = J Clin Invest | volume = 99 | issue = 10| pages = 2391–7 | pmid = 9153281 | doi = 10.1172/JCI119421 | pmc = 508078 | date = May 1997 }}</ref>
==Diagnosis==

{{Empty section|date=October 2024}}
⚫
==Presentation==
⚫
Sufferers have unusually high concentrations of xanthine in their blood and urine, which can lead to health problems such as [[renal failure]] and xanthine kidney stones, one of the rarest types of kidney stones.


==Treatment==
==Treatment==
There is no specific treatment beyond maintaining a high fluid intake and avoiding foods that are high in [[purine]].
There is no specific treatment beyond maintaining a high fluid intake and avoiding foods that are high in [[purine]].{{cn|date=October 2024}}


==References==
==References==
{{reflist}}
<references/>
{{refbegin}}
<div class="references-small">
* {{cite journal|author1=Kojima T. |author2=Nishina T. |author3=Kitamura M. |author4=Hosoya T. |author5=Nishioka K. | title = Biochemical studies on the purine metabolism of four cases with hereditary xanthinuria| journal= Clin Chim Acta| year= 1984| volume = 137| issue = 2| pages= 189–98| pmid = 6423323| doi = 10.1016/0009-8981(84)90179-7}}
*{{cite journal
* {{cite journal| author = Hille R.| title = Structure and Function of Xanthine Oxidoreductase| journal= [[European Journal of Inorganic Chemistry]]| year = 2006| volume = 2006| issue = 10| pages= 1905–2095| doi = 10.1002/ejic.200600087}}{{refend}}
| author = Kojima T., Nishina T., Kitamura M., Hosoya T., Nishioka K.
| title = Biochemical studies on the purine metabolism of four cases with hereditary xanthinuria
| journal= Clin Chim Acta.
| year= 1984
| volume = 137
| issue = 2
| pages= 189–98
| pmid = 6423323
| doi = 10.1016/0009-8981(84)90179-7}}


⚫
== External links ==
*{{cite journal
{{Medical resources
| author = Hille R.
| ICD10 = {{ICD10|E|79|8|e|70}}
| title = Structure and Function of Xanthine Oxidoreductase
| ICD9 = {{ICD9|277.2}}
| journal= [[European Journal of Inorganic Chemistry]]
| ICDO =
| year = 2006
| OMIM = 278300
| volume = 2006
⚫
| OMIM_mult = {{OMIM|603592||none}}
| issue = 10
| MedlinePlus =
| pages= 1905–2095
⚫
| eMedicineSubj = ped
| doi = 10.1002/ejic.200600087}}</div>
⚫
| eMedicineTopic = 2452

| DiseasesDB = 14194
⚫
==External links==
| SNOMED CT = 190919008
*{{GPnotebook|644546576}}
}}
*{{RareDiseases|5621|Xanthinuria}}
* {{RareDiseases|5621|Xanthinuria}}


{{Purine, pyrimidine, porphyrin, bilirubin metabolic pathology}}
{{Purine, pyrimidine, porphyrin, bilirubin metabolic pathology}}
{{Purinergics}}


[[Category:Inborn errors of purine-pyrimidine metabolism]]
[[Category:Inborn errors of purine-pyrimidine metabolism]]

[[de:Xanthinurie]]
[[fr:Xanthinurie]]
[[it:Xantinuria]]
[[pl:Ksantynuria]]

Latest revision as of 20:20, 30 October 2024

Xanthinuria
Xanthine
SpecialtyEndocrinology Edit this on Wikidata

Xanthinuria, also known as xanthine oxidase deficiency, is a rare genetic disorder causing the accumulation of xanthine. It is caused by a deficiency of the enzyme xanthine oxidase.

It was first formally characterized in 1954.[1]

Presentation

[edit]

Affected people have unusually high concentrations of xanthine in their blood and urine, which can lead to health problems such as renal failure and xanthine kidney stones, one of the rarest types of kidney stones.[citation needed]

Causes

[edit]

Type I xanthinuria can be caused by a deficiency of xanthine oxidase, which is an enzyme necessary for converting xanthine to uric acid.[2] Type II xanthinuria and molybdenum cofactor deficiency lack one or two other enzyme activities in addition to xanthine oxidase.[3]

Diagnosis

[edit]

Treatment

[edit]

There is no specific treatment beyond maintaining a high fluid intake and avoiding foods that are high in purine.[citation needed]

References

[edit]
  1. ^ Dent CE, Philpot GR (1954). "Xanthinuria, an inborn error (or deviation) of metabolism". Lancet. 266 (6804): 182–5. doi:10.1016/S0140-6736(54)91257-X. PMID 13118765.
  2. ^ Ichida K, Amaya Y, Kamatani N, Nishino T, Hosoya T, Sakai O (1997). "Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria". J. Clin. Invest. 99 (10): 2391–7. doi:10.1172/JCI119421. PMC 508078. PMID 9153281.
  3. ^ Ichida K, Amaya Y, Kamatani N, Nishino T, Hosoya T, Sakai O (May 1997). "Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria". J Clin Invest. 99 (10): 2391–7. doi:10.1172/JCI119421. PMC 508078. PMID 9153281.{{cite journal}}: CS1 maint: multiple names: authors list (link)
[edit]
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