Menkes disease (patient information): Difference between revisions
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==Overview== | |||
== | |||
[[Menkes syndrome]] is an [[inborn error of metabolism]] in which [[cells]] in the [[body]] cannot absorb enough [[copper]]. | [[Menkes syndrome]] is an [[inborn error of metabolism]] in which [[cells]] in the [[body]] cannot absorb enough [[copper]]. | ||
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==Who is at risk for Menkes disease?== | ==Who is at risk for Menkes disease?== | ||
[[Menkes disease]] is a [[genetic disorder]], so anyone with a [[family history]] of the [[disease]] is at risk. | |||
== | ==When to seek urgent medical care?== | ||
Talk to your [[health care provider]] if you have a [[family history]] of [[Menkes syndrome]] and you plan to have children. A baby with this [[condition]] will often show symptoms early in [[infancy]]. | |||
==Diagnosis== | |||
There is often a history of [[Menkes syndrome]] in a [[male]] relative. | There is often a history of [[Menkes syndrome]] in a [[male]] relative. | ||
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[[Genetic testing]] may show a change ([[mutation]]) in the [[ATP7A]] [[gene]]. | [[Genetic testing]] may show a change ([[mutation]]) in the [[ATP7A]] [[gene]]. | ||
==Treatment options== | ==Treatment options== | ||
[[Treatment]] usually only helps when started very early in the course of the [[disease]]. [[Injections]] of [[copper]] into a [[vein]] or under the [[skin]] have been used with mixed results. | |||
==Where to find medical care for Menkes disease== | ==Where to find medical care for Menkes disease?== | ||
[http://maps.google.com/maps?f=q&hl=en&geocode=&q={{urlencode:{{#if:{{{1|}}}|{{{1}}}|Menkes disease}}}}&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 Menkes disease] | [http://maps.google.com/maps?f=q&hl=en&geocode=&q={{urlencode:{{#if:{{{1|}}}|{{{1}}}|Menkes disease}}}}&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 Menkes disease] | ||
==What to expect (Outlook/Prognosis)== | ==What to expect (Outlook/Prognosis)?== | ||
Most persons with this [[condition]] die within the first few years of life. | |||
==Possible complications== | ==Possible complications== | ||
*[[Seizures]] | |||
*[[Death]] | |||
==Sources== | ==Sources== | ||
http://www.nlm.nih.gov/medlineplus/ency/article/001160.htm | http://www.nlm.nih.gov/medlineplus/ency/article/001160.htm | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
[[Category:Patient | |||
[[Category:Mature chapter]] | |||
[[Category:Disease]] | |||
[[Category:Syndromes]] | |||
[[Category:Patient information]] | |||
[[Category:Genetic disorders]] | |||
[[Category:Genetic disorders patient information]] |
Latest revision as of 17:19, 9 August 2012
For the WikiDoc page for this topic, click here
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Assistant Editor-in-Chief: Alexandra M. Palmer
Overview
Menkes syndrome is an inborn error of metabolism in which cells in the body cannot absorb enough copper.
What are the symptoms of Menkes disease?
- Bone spurs
- Brittle, kinky hair
- Feeding difficulties
- Irritability
- Lack of muscle tone, floppiness (hypotonia)
- Low body temperature
- Mental deterioration
- Pudgy, rosy cheeks
- Seizures
- Skeletal changes
What causes Menkes disease?
Menkes syndrome is caused by a defect in the ATP7A gene. The defect makes it hard for the body to distribute and absorb copper. As a result, the brain and other parts of the body do not get enough copper.
Low copper levels can affect the structure of bone, skin, hair, and blood vessels and interfere with nerve function. Copper also builds up in the small intestine and kidneys.
Menkes syndrome is inherited, which means it runs in families.
Who is at risk for Menkes disease?
Menkes disease is a genetic disorder, so anyone with a family history of the disease is at risk.
When to seek urgent medical care?
Talk to your health care provider if you have a family history of Menkes syndrome and you plan to have children. A baby with this condition will often show symptoms early in infancy.
Diagnosis
There is often a history of Menkes syndrome in a male relative.
Signs include:
- Abnormal appearance of the hair under the microscope
- Abnormally low body temperature
- Bleeding in the brain
- Slow growth in the womb
In males, all of the hairs will be abnormal. In females who carry this trait, only half of the hairs may be abnormal.
Tests include:
- Serum ceruloplasmin
- Serum copper level
- Skin cell (fibroblast) culture
- X-ray of the skeleton or x-ray of the skull
Genetic testing may show a change (mutation) in the ATP7A gene.
Treatment options
Treatment usually only helps when started very early in the course of the disease. Injections of copper into a vein or under the skin have been used with mixed results.
Where to find medical care for Menkes disease?
Directions to Hospitals Treating Menkes disease
What to expect (Outlook/Prognosis)?
Most persons with this condition die within the first few years of life.