3q29 microdeletion syndrome: Difference between revisions
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{{Short description|A genetic disorder caused by a deletion on chromosome 3}} | {{Short description|A genetic disorder caused by a deletion on chromosome 3}} | ||
{{Medical genetics}} | {{Infobox medical condition | ||
| name = 3q29 microdeletion syndrome | |||
| image = [[File:Human_male_karyotpe_high_resolution_-_Chromosome_3_cropped.png]] | |||
| caption = Chromosome 3 | |||
| width = | |||
| synonyms = | |||
| pronounce = | |||
| specialty = [[Medical genetics]] | |||
| symptoms = [[Developmental delay]], [[intellectual disability]], [[autism spectrum disorder]], [[anxiety]], [[schizophrenia]] | |||
| onset = [[Congenital]] | |||
| duration = Lifelong | |||
| types = | |||
| causes = [[Genetic mutation]] | |||
| risks = | |||
| diagnosis = [[Genetic testing]], [[chromosomal microarray analysis]] | |||
| differential = | |||
| prevention = | |||
| treatment = [[Supportive care]], [[special education]], [[behavioral therapy]] | |||
| medication = | |||
| prognosis = Variable | |||
| frequency = 1 in 30,000 to 1 in 40,000 | |||
| deaths = | |||
}} | |||
'''3q29 microdeletion syndrome''' is a rare genetic disorder characterized by a deletion of a small segment of chromosome 3 at the q29 band. This condition can lead to a variety of developmental and health issues, including intellectual disability, developmental delay, and distinctive facial features. | '''3q29 microdeletion syndrome''' is a rare genetic disorder characterized by a deletion of a small segment of chromosome 3 at the q29 band. This condition can lead to a variety of developmental and health issues, including intellectual disability, developmental delay, and distinctive facial features. | ||
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* [[Genetic disorder]] | * [[Genetic disorder]] | ||
* [[Intellectual disability]] | * [[Intellectual disability]] | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Rare diseases]] | [[Category:Rare diseases]] | ||
[[Category:Chromosomal disorders]] | [[Category:Chromosomal disorders]] | ||
{{genetics-stub}} | |||
Latest revision as of 04:18, 25 March 2025
A genetic disorder caused by a deletion on chromosome 3
| 3q29 microdeletion syndrome | |
|---|---|
| |
| Synonyms | |
| Pronounce | |
| Specialty | Medical genetics |
| Symptoms | Developmental delay, intellectual disability, autism spectrum disorder, anxiety, schizophrenia |
| Complications | N/A |
| Onset | Congenital |
| Duration | Lifelong |
| Types | |
| Causes | Genetic mutation |
| Risks | |
| Diagnosis | Genetic testing, chromosomal microarray analysis |
| Differential diagnosis | |
| Prevention | |
| Treatment | Supportive care, special education, behavioral therapy |
| Medication | |
| Prognosis | Variable |
| Frequency | 1 in 30,000 to 1 in 40,000 |
| Deaths | |
3q29 microdeletion syndrome is a rare genetic disorder characterized by a deletion of a small segment of chromosome 3 at the q29 band. This condition can lead to a variety of developmental and health issues, including intellectual disability, developmental delay, and distinctive facial features.
Genetics[edit]
The 3q29 microdeletion syndrome is caused by the deletion of a segment of DNA on the long arm (q arm) of chromosome 3. This deletion typically spans approximately 1.6 million base pairs and affects multiple genes. The deletion is usually de novo, meaning it occurs as a new mutation in the affected individual and is not inherited from the parents.
Clinical Features[edit]
Individuals with 3q29 microdeletion syndrome may present with a range of clinical features, which can vary in severity. Common features include:
- Intellectual disability
- Developmental delay
- Autism spectrum disorder
- Microcephaly (small head size)
- Distinctive facial features such as a long face, high nasal bridge, and prominent ears
- Congenital heart defects
- Gastrointestinal issues
Diagnosis[edit]
Diagnosis of 3q29 microdeletion syndrome is typically made using chromosomal microarray analysis, which can detect the deletion of the 3q29 region. Karyotyping may also be used, but it is less sensitive for detecting small deletions.
Management[edit]
There is no cure for 3q29 microdeletion syndrome, and management focuses on addressing the specific symptoms and needs of the individual. This may include:
- Early intervention programs for developmental delays
- Special education services
- Behavioral therapy for autism spectrum disorder
- Regular monitoring and treatment of associated health issues
Prognosis[edit]
The prognosis for individuals with 3q29 microdeletion syndrome varies depending on the severity of symptoms and the presence of associated health conditions. With appropriate support and interventions, many individuals can lead fulfilling lives.
Related pages[edit]
