Alkaptonuria (patient information): Difference between revisions
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{{ | {{Template:Alkaptonuria (patient information)}} | ||
''' | '''For the WikiDoc page for this topic, click [[Alkaptonuria|here]]''' | ||
{{ | {{CMG}}; '''Assistant Editor(s)-in-Chief:''' Katherine Ogando | ||
==Overview== | |||
[[Alkaptonuria]] is a rare condition in which a person's urine turns a dark brownish-black color when exposed to air. | |||
== | |||
Alkaptonuria is a rare condition in which a person's urine turns a dark brownish-black color when exposed to air. | |||
==What are the symptoms of Alkaptonuria?== | ==What are the symptoms of Alkaptonuria?== | ||
Urine in an infant's diaper may darken and can turn almost black after several hours. However, many persons with this condition may not know they have it until mid-adulthood (around age 40), when joint and other problems occur. | Urine in an infant's diaper may darken and can turn almost black after several hours. However, many persons with this condition may not know they have it until mid-adulthood (around age 40), when [[joint]] and other problems occur. | ||
Symptoms may include: | Symptoms may include: | ||
* Arthritis (especially of the spine) that gets worse over time | * [[Arthritis]] (especially of the spine) that gets worse over time | ||
* Darkening of the ear | * Darkening of the [[ear]] | ||
* Dark spots on the white of the eye (sclera) and cornea | * Dark spots on the white of the eye ([[sclera]]) and [[cornea]] | ||
==What causes Alkaptonuria?== | |||
A defect in the HGD gene causes alkaptonuria. | |||
The gene defect makes the body unable to properly break down certain amino acids (tyrosine and phenylalanine). As a result, a substance called homogentisic acid builds up in the skin and other body tissues. The acid leaves the body through the urine. The urine turns brownish-black when it mixes with air. | |||
Alkaptonuria is inherited, which means it is passed down from parents to their children. To get this disease, each of your parents must pass you a copy of the faulty HGD gene. | |||
==When to seek urgent medical care== | ==When to seek urgent medical care?== | ||
Call your health care provider if you notice that your own urine or your child's urine becomes dark brown or black when it is exposed to air. | Call your health care provider if you notice that your own urine or your child's urine becomes dark brown or black when it is exposed to air. | ||
==Diagnosis== | |||
A urine test ([[urinalysis]]) is done to test for [[alkaptonuria]]. If ferric chloride is added to the urine, it will turn the urine a black color in patients with this condition. | |||
==Treatment options== | ==Treatment options== | ||
Some patients benefit from high-dose vitamin C. This has been shown to decrease the build-up of brown pigment in the cartilage and may slow the development of arthritis. | Some patients benefit from high-dose [[vitamin C]]. This has been shown to decrease the build-up of brown pigment in the cartilage and may slow the development of [[arthritis]]. | ||
==Diseases with similar symptoms== | ==Diseases with similar symptoms== | ||
* Ankylosing Spondylitis | * [[Ankylosing spondylitis (patient informtion)|Ankylosing Spondylitis]] | ||
* Acute intermittent porphyria | * Acute intermittent [[porphyria]] | ||
==Where to find medical care for Alkaptonuria== | ==Where to find medical care for Alkaptonuria?== | ||
[http://maps.google.com/maps?f=q&hl=en&geocode=&q={{urlencode:{{#if:{{{1|}}}|{{{1}}}|Alkaptonuria}}}}&sll=37.0625,-95.677068&sspn=65.008093,112.148438&ie=UTF8&ll=37.0625,-95.677068&spn=91.690419,149.414063&z=2&source=embed Directions to Hospitals Treating Alkaptonuria] | [http://maps.google.com/maps?f=q&hl=en&geocode=&q={{urlencode:{{#if:{{{1|}}}|{{{1}}}|Alkaptonuria}}}}&sll=37.0625,-95.677068&sspn=65.008093,112.148438&ie=UTF8&ll=37.0625,-95.677068&spn=91.690419,149.414063&z=2&source=embed Directions to Hospitals Treating Alkaptonuria] | ||
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There is no know prevention of alkaptonuria. | There is no know prevention of alkaptonuria. | ||
==What to expect (Outlook/Prognosis)== | ==What to expect (Outlook/Prognosis)?== | ||
The outcome for people affected with alkaptonuria is generally expected to be good. Some possible complications include people with this condition also can get arthritis in adulthood. The build-up of homogentisic acid in the cartilage causes arthritis in about 50% of older adults with alkaptonuria. | The outcome for people affected with alkaptonuria is generally expected to be good. Some possible complications include people with this condition also can get [[arthritis]] in adulthood. The build-up of [[homogentisic acid]] in the [[cartilage]] causes arthritis in about 50% of older adults with alkaptonuria. | ||
* Homogentisic acid also can build up on the heart valves, especially the mitral valve. This can sometimes lead to the need for valve replacement. | * [[Homogentisic acid]] also can build up on the heart valves, especially the mitral valve. This can sometimes lead to the need for valve replacement. | ||
* Coronary artery disease may develop earlier in people with alkaptonuria. | * Coronary artery disease may develop earlier in people with alkaptonuria. | ||
* Kidney stones and prostate stones may be more common in people with alkaptonuria. | * [[Kidney stones]] and [[prostate stones]] may be more common in people with alkaptonuria. | ||
== | ==Possible complications== | ||
People with this condition also can get arthritis in adulthood. The build-up of homogentisic acid in the cartilage causes arthritis in about 50% of older adults with alkaptonuria. | |||
*Homogentisic acid also can build up on the heart valves, especially the mitral valve. This can sometimes lead to the need for valve replacement. | |||
*[[Coronary heart disease (patient information)|Coronary artery disease]] may develop earlier in people with alkaptonuria. | |||
*Kidney stones and prostate stones may be more common in people with alkaptonuria. | |||
==Sources== | |||
[http://www.nlm.nih.gov/medlineplus/ency/article/001200.htm Medline Plus: Alkaptonuria] | |||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
[[Category:Patient | |||
[[Category:Patient information]] | |||
[[Category:Genetic disorders]] | |||
[[Category:Inborn errors of metabolism]] | |||
[[Category:Genetic disorders patient information]] | |||
[[Category:Overview complete]] | |||
[[Category:Disease]] | |||
[[Category:Metabolic disorders]] | |||
[[Category:Metabolic disorders patient information]] | |||
[[Category:Template complete]] | |||
Latest revision as of 18:32, 17 April 2012
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Alkaptonuria |
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Alkaptonuria On the Web |
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For the WikiDoc page for this topic, click here
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Assistant Editor(s)-in-Chief: Katherine Ogando
Overview
Alkaptonuria is a rare condition in which a person's urine turns a dark brownish-black color when exposed to air.
What are the symptoms of Alkaptonuria?
Urine in an infant's diaper may darken and can turn almost black after several hours. However, many persons with this condition may not know they have it until mid-adulthood (around age 40), when joint and other problems occur.
Symptoms may include:
- Arthritis (especially of the spine) that gets worse over time
- Darkening of the ear
- Dark spots on the white of the eye (sclera) and cornea
What causes Alkaptonuria?
A defect in the HGD gene causes alkaptonuria.
The gene defect makes the body unable to properly break down certain amino acids (tyrosine and phenylalanine). As a result, a substance called homogentisic acid builds up in the skin and other body tissues. The acid leaves the body through the urine. The urine turns brownish-black when it mixes with air.
Alkaptonuria is inherited, which means it is passed down from parents to their children. To get this disease, each of your parents must pass you a copy of the faulty HGD gene.
When to seek urgent medical care?
Call your health care provider if you notice that your own urine or your child's urine becomes dark brown or black when it is exposed to air.
Diagnosis
A urine test (urinalysis) is done to test for alkaptonuria. If ferric chloride is added to the urine, it will turn the urine a black color in patients with this condition.
Treatment options
Some patients benefit from high-dose vitamin C. This has been shown to decrease the build-up of brown pigment in the cartilage and may slow the development of arthritis.
Diseases with similar symptoms
- Ankylosing Spondylitis
- Acute intermittent porphyria
Where to find medical care for Alkaptonuria?
Directions to Hospitals Treating Alkaptonuria
Prevention of Alkaptonuria
There is no know prevention of alkaptonuria.
What to expect (Outlook/Prognosis)?
The outcome for people affected with alkaptonuria is generally expected to be good. Some possible complications include people with this condition also can get arthritis in adulthood. The build-up of homogentisic acid in the cartilage causes arthritis in about 50% of older adults with alkaptonuria.
- Homogentisic acid also can build up on the heart valves, especially the mitral valve. This can sometimes lead to the need for valve replacement.
- Coronary artery disease may develop earlier in people with alkaptonuria.
- Kidney stones and prostate stones may be more common in people with alkaptonuria.
Possible complications
People with this condition also can get arthritis in adulthood. The build-up of homogentisic acid in the cartilage causes arthritis in about 50% of older adults with alkaptonuria.
- Homogentisic acid also can build up on the heart valves, especially the mitral valve. This can sometimes lead to the need for valve replacement.
- Coronary artery disease may develop earlier in people with alkaptonuria.
- Kidney stones and prostate stones may be more common in people with alkaptonuria.