Immunodeficiency–centromeric instability–facial anomalies syndrome: Difference between revisions
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[[File:Autosomal_recessive_-_en.svg| | {{SI}} | ||
{{Infobox medical condition | |||
| name = Immunodeficiency–centromeric instability–facial anomalies syndrome | |||
| image = [[File:Autosomal_recessive_-_en.svg|200px]] | |||
| caption = This condition is inherited in an [[autosomal recessive]] pattern. | |||
| synonyms = ICF syndrome | |||
| pronounce = | |||
| specialty = [[Medical genetics]] | |||
| symptoms = [[Immunodeficiency]], [[centromeric instability]], [[facial anomalies]] | |||
| onset = | |||
| duration = | |||
| types = | |||
| causes = Mutations in the [[DNMT3B]] gene | |||
| risks = | |||
| diagnosis = [[Genetic testing]], [[clinical evaluation]] | |||
| differential = | |||
| prevention = | |||
| treatment = [[Immunoglobulin replacement therapy]], [[antibiotics]] | |||
| medication = | |||
| prognosis = Variable, depending on severity | |||
| frequency = Rare | |||
| deaths = | |||
}} | |||
'''Immunodeficiency–centromeric instability–facial anomalies syndrome''' (ICF syndrome) is a rare [[genetic disorder]] characterized by a combination of [[immunodeficiency]], [[centromeric instability]], and distinctive [[facial anomalies]]. The syndrome is caused by mutations in genes involved in [[DNA methylation]] and chromatin structure, leading to defects in [[chromosome]] stability and immune function. | |||
== Clinical Features == | == Clinical Features == | ||
Individuals with ICF syndrome typically present with: | Individuals with ICF syndrome typically present with: | ||
* | * '''Immunodeficiency''': Recurrent infections due to low levels of [[immunoglobulins]] and impaired function of [[B cells]] and [[T cells]]. | ||
* | * '''Centromeric instability''': Chromosomal abnormalities, particularly involving chromosomes 1, 9, and 16, which can be observed in [[karyotype]] analysis. | ||
* | * '''Facial anomalies''': Distinctive facial features such as a flat nasal bridge, epicanthal folds, and a high-arched palate. | ||
== Genetics == | == Genetics == | ||
ICF syndrome is primarily associated with mutations in the [[DNMT3B]] gene, which encodes a [[DNA methyltransferase]] involved in the establishment of DNA methylation patterns. Other genes implicated in the syndrome include [[ZBTB24]], [[CDCA7]], and [[HELLS]]. The inheritance pattern of ICF syndrome is typically [[autosomal recessive]]. | ICF syndrome is primarily associated with mutations in the [[DNMT3B]] gene, which encodes a [[DNA methyltransferase]] involved in the establishment of DNA methylation patterns. Other genes implicated in the syndrome include [[ZBTB24]], [[CDCA7]], and [[HELLS]]. The inheritance pattern of ICF syndrome is typically [[autosomal recessive]]. | ||
== Diagnosis == | == Diagnosis == | ||
Diagnosis of ICF syndrome involves a combination of clinical evaluation, immunological testing, and genetic analysis. Key diagnostic criteria include: | Diagnosis of ICF syndrome involves a combination of clinical evaluation, immunological testing, and genetic analysis. Key diagnostic criteria include: | ||
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* Chromosomal analysis showing centromeric instability. | * Chromosomal analysis showing centromeric instability. | ||
* Genetic testing confirming mutations in the DNMT3B gene or other related genes. | * Genetic testing confirming mutations in the DNMT3B gene or other related genes. | ||
== Management == | == Management == | ||
Management of ICF syndrome focuses on treating infections and supporting the immune system. This may include: | Management of ICF syndrome focuses on treating infections and supporting the immune system. This may include: | ||
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* Prophylactic antibiotics to prevent infections. | * Prophylactic antibiotics to prevent infections. | ||
* Hematopoietic stem cell transplantation (HSCT) in severe cases. | * Hematopoietic stem cell transplantation (HSCT) in severe cases. | ||
== Prognosis == | == Prognosis == | ||
The prognosis for individuals with ICF syndrome varies depending on the severity of the immunodeficiency and the effectiveness of treatment. Early diagnosis and appropriate management can improve outcomes and quality of life. | The prognosis for individuals with ICF syndrome varies depending on the severity of the immunodeficiency and the effectiveness of treatment. Early diagnosis and appropriate management can improve outcomes and quality of life. | ||
== See also == | |||
== | |||
* [[Immunodeficiency]] | * [[Immunodeficiency]] | ||
* [[Chromosome instability]] | * [[Chromosome instability]] | ||
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* [[Autosomal recessive]] | * [[Autosomal recessive]] | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Immunodeficiency]] | [[Category:Immunodeficiency]] | ||
[[Category:Rare diseases]] | [[Category:Rare diseases]] | ||
{{Genetic-disorder-stub}} | {{Genetic-disorder-stub}} | ||
{{medicine-stub}} | {{medicine-stub}} | ||
Latest revision as of 22:27, 8 April 2025
Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC
| Immunodeficiency–centromeric instability–facial anomalies syndrome | |
|---|---|
| |
| Synonyms | ICF syndrome |
| Pronounce | |
| Specialty | Medical genetics |
| Symptoms | Immunodeficiency, centromeric instability, facial anomalies |
| Complications | N/A |
| Onset | |
| Duration | |
| Types | |
| Causes | Mutations in the DNMT3B gene |
| Risks | |
| Diagnosis | Genetic testing, clinical evaluation |
| Differential diagnosis | |
| Prevention | |
| Treatment | Immunoglobulin replacement therapy, antibiotics |
| Medication | |
| Prognosis | Variable, depending on severity |
| Frequency | Rare |
| Deaths | |
Immunodeficiency–centromeric instability–facial anomalies syndrome (ICF syndrome) is a rare genetic disorder characterized by a combination of immunodeficiency, centromeric instability, and distinctive facial anomalies. The syndrome is caused by mutations in genes involved in DNA methylation and chromatin structure, leading to defects in chromosome stability and immune function.
Clinical Features[edit]
Individuals with ICF syndrome typically present with:
- Immunodeficiency: Recurrent infections due to low levels of immunoglobulins and impaired function of B cells and T cells.
- Centromeric instability: Chromosomal abnormalities, particularly involving chromosomes 1, 9, and 16, which can be observed in karyotype analysis.
- Facial anomalies: Distinctive facial features such as a flat nasal bridge, epicanthal folds, and a high-arched palate.
Genetics[edit]
ICF syndrome is primarily associated with mutations in the DNMT3B gene, which encodes a DNA methyltransferase involved in the establishment of DNA methylation patterns. Other genes implicated in the syndrome include ZBTB24, CDCA7, and HELLS. The inheritance pattern of ICF syndrome is typically autosomal recessive.
Diagnosis[edit]
Diagnosis of ICF syndrome involves a combination of clinical evaluation, immunological testing, and genetic analysis. Key diagnostic criteria include:
- Reduced levels of serum immunoglobulins (IgG, IgA, and IgM).
- Chromosomal analysis showing centromeric instability.
- Genetic testing confirming mutations in the DNMT3B gene or other related genes.
Management[edit]
Management of ICF syndrome focuses on treating infections and supporting the immune system. This may include:
- Regular administration of intravenous immunoglobulin (IVIG) to boost immune function.
- Prophylactic antibiotics to prevent infections.
- Hematopoietic stem cell transplantation (HSCT) in severe cases.
Prognosis[edit]
The prognosis for individuals with ICF syndrome varies depending on the severity of the immunodeficiency and the effectiveness of treatment. Early diagnosis and appropriate management can improve outcomes and quality of life.
See also[edit]
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