Beckwith-Wiedemann Syndrome: Difference between revisions
From WikiLectures
m (typo) |
mNo edit summary |
||
| (3 intermediate revisions by 3 users not shown) | |||
| Line 10: | Line 10: | ||
* | * | ||
* This warning note is automatically inserted by inserting the template {{subst:Inserted article}}. | * This warning note is automatically inserted by inserting the template {{subst:Inserted article}}. | ||
--------------------------------------------------------------------------------------------------------------> | -------------------------------------------------------------------------------------------------------------->__NOTOC__<noinclude>{{Dictionary | ||
__NOTOC__<noinclude>{{Dictionary | |||
|eng=Beckwith-Wiedemann syndrome}}</noinclude> | |eng=Beckwith-Wiedemann syndrome}}</noinclude> | ||
* This uniparental disomy is connected with '''changes of methylation on chromosome 11'''. The syndrome affects more parts of the body. | * This uniparental disomy is connected with '''changes of methylation on chromosome 11 (11p15)'''. The syndrome affects more parts of the body. | ||
* ''Typical symptoms'': macrosomia (overgrowth), omphalocele ( | * ''Typical symptoms'': macrosomia (overgrowth or simply [[gigantism]]), omphalocele (or related abdominall wall defect), large [[tongue]] ([[macroglossia]]), [[kidney]] abnormalities, [[hypoglycemia]] (because of the hyperinsulinisms) and increased risk of tumors (like [[Wilms tumor]]) during the childhood. About 20% of patients die in early age because of the complications of these congenital symptoms. | ||
* It is alo called '''EMG syndrome''' ('''e'''xomphalos, '''m'''acroglossia, '''g'''igantism). | |||
* Incidence of Beckwith-Wiedemann sydrome is ''1 in 12 000 people'' worldwide. | * Incidence of Beckwith-Wiedemann sydrome is ''1 in 12 000 people'' worldwide. | ||
* Molecular-genetic diagnostics (inluding the identification of abnormal methylation) is possible. | |||
<noinclude> | <noinclude> | ||
== Links == | == Links == | ||
=== Related articles === | === Related articles === | ||
| Line 23: | Line 25: | ||
* [[Allele]] | * [[Allele]] | ||
* [[Chromosome]] | * [[Chromosome]] | ||
=== Sources=== | === Sources === | ||
* [http://ghr.nlm.nih.gov/handbook/inheritance/updimprinting What are Genomic Imprinting and Uniparental Disomy] | * [http://ghr.nlm.nih.gov/handbook/inheritance/updimprinting What are Genomic Imprinting and Uniparental Disomy] | ||
* [http://www.geneimprint.com/site/what-is-imprinting What is Genomic Imprinting?] | * [http://www.geneimprint.com/site/what-is-imprinting What is Genomic Imprinting?] | ||
| Line 38: | Line 40: | ||
</noinclude> | </noinclude> | ||
[[Category: Biology]] | [[Category:Inserted articles]] | ||
[[Category: Genetics]] | [[Category:Biology]] | ||
[[Category:Genetics]] | |||
[[Category:Paediatrics]] | |||
Latest revision as of 10:11, 23 December 2023
| English: Beckwith-Wiedemann syndrome |  |
- This uniparental disomy is connected with changes of methylation on chromosome 11 (11p15). The syndrome affects more parts of the body.
- Typical symptoms: macrosomia (overgrowth or simply gigantism), omphalocele (or related abdominall wall defect), large tongue (macroglossia), kidney abnormalities, hypoglycemia (because of the hyperinsulinisms) and increased risk of tumors (like Wilms tumor) during the childhood. About 20% of patients die in early age because of the complications of these congenital symptoms.
- It is alo called EMG syndrome (exomphalos, macroglossia, gigantism).
- Incidence of Beckwith-Wiedemann sydrome is 1 in 12 000 people worldwide.
- Molecular-genetic diagnostics (inluding the identification of abnormal methylation) is possible.
Links[edit | edit source]
Related articles[edit | edit source]
Sources[edit | edit source]
Bibliography[edit | edit source]
- KUMAR, ABBAS, FAUSTO, MITCHELL,. Robbins Basic Pathology. 8th edition edition. 2007. ISBN 978-0-8089-2366-4.
