Knobloch syndrome: Difference between revisions
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{{Infobox medical condition | |||
| name = Knobloch syndrome | |||
| synonyms = | |||
| pronounce = | |||
| image = | |||
| alt = | |||
| caption = | |||
| field = [[Medical genetics]] | |||
| symptoms = [[Retinal detachment]], [[vitreous]] abnormalities, [[encephalocele]] | |||
| complications = [[Vision loss]], [[neurological complications]] | |||
| onset = Congenital | |||
| duration = Lifelong | |||
| types = | |||
| causes = [[Genetic mutation]] | |||
| risks = | |||
| diagnosis = [[Genetic testing]], [[ophthalmologic examination]] | |||
| differential = | |||
| prevention = | |||
| treatment = [[Surgical intervention]], [[supportive care]] | |||
| medication = | |||
| prognosis = Variable, depending on severity | |||
| frequency = Rare | |||
| deaths = | |||
}} | |||
'''Knobloch syndrome''' is a rare genetic disorder characterized by a combination of ocular and cranial abnormalities. It is named after the German ophthalmologist [[Werner Knobloch]], who first described the condition. The syndrome is primarily associated with mutations in the [[COL18A1]] gene, which encodes the protein collagen XVIII. | '''Knobloch syndrome''' is a rare genetic disorder characterized by a combination of ocular and cranial abnormalities. It is named after the German ophthalmologist [[Werner Knobloch]], who first described the condition. The syndrome is primarily associated with mutations in the [[COL18A1]] gene, which encodes the protein collagen XVIII. | ||
== Clinical Features == | == Clinical Features == | ||
Individuals with Knobloch syndrome typically present with a range of symptoms, including: | Individuals with Knobloch syndrome typically present with a range of symptoms, including: | ||
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* [[Cranial abnormalities]], such as occipital encephalocele or [[microcephaly]] | * [[Cranial abnormalities]], such as occipital encephalocele or [[microcephaly]] | ||
* [[Intellectual disability]] in some cases | * [[Intellectual disability]] in some cases | ||
== Genetics == | == Genetics == | ||
Knobloch syndrome is inherited in an [[autosomal recessive]] manner. This means that an individual must inherit two copies of the mutated gene, one from each parent, to manifest the disorder. The primary gene implicated in Knobloch syndrome is [[COL18A1]], which is located on chromosome 21. | Knobloch syndrome is inherited in an [[autosomal recessive]] manner. This means that an individual must inherit two copies of the mutated gene, one from each parent, to manifest the disorder. The primary gene implicated in Knobloch syndrome is [[COL18A1]], which is located on chromosome 21. | ||
== Diagnosis == | == Diagnosis == | ||
Diagnosis of Knobloch syndrome is based on clinical evaluation, family history, and genetic testing. [[Ophthalmologic]] examination is crucial for identifying the characteristic eye abnormalities. [[Neuroimaging]] techniques, such as [[MRI]] or [[CT scan]], may be used to detect cranial defects. | Diagnosis of Knobloch syndrome is based on clinical evaluation, family history, and genetic testing. [[Ophthalmologic]] examination is crucial for identifying the characteristic eye abnormalities. [[Neuroimaging]] techniques, such as [[MRI]] or [[CT scan]], may be used to detect cranial defects. | ||
== Management == | == Management == | ||
There is no cure for Knobloch syndrome, and treatment is primarily supportive. Management strategies may include: | There is no cure for Knobloch syndrome, and treatment is primarily supportive. Management strategies may include: | ||
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* Special education services for individuals with intellectual disabilities | * Special education services for individuals with intellectual disabilities | ||
* Genetic counseling for affected families | * Genetic counseling for affected families | ||
== Epidemiology == | == Epidemiology == | ||
Knobloch syndrome is extremely rare, with only a few hundred cases reported worldwide. The exact prevalence is unknown due to the rarity of the condition and potential underdiagnosis. | Knobloch syndrome is extremely rare, with only a few hundred cases reported worldwide. The exact prevalence is unknown due to the rarity of the condition and potential underdiagnosis. | ||
== See Also == | == See Also == | ||
* [[COL18A1]] | * [[COL18A1]] | ||
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* [[Autosomal recessive]] | * [[Autosomal recessive]] | ||
* [[Genetic counseling]] | * [[Genetic counseling]] | ||
== References == | == References == | ||
{{Reflist}} | {{Reflist}} | ||
== External Links == | == External Links == | ||
{{No external links}} | {{No external links}} | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Ophthalmology]] | [[Category:Ophthalmology]] | ||
[[Category:Neurology]] | [[Category:Neurology]] | ||
[[Category:Rare diseases]] | [[Category:Rare diseases]] | ||
{{Genetics-stub}} | {{Genetics-stub}} | ||
{{No image}} | {{No image}} | ||
Latest revision as of 00:27, 4 April 2025
| Knobloch syndrome | |
|---|---|
| Synonyms | |
| Pronounce | |
| Specialty | N/A |
| Symptoms | Retinal detachment, vitreous abnormalities, encephalocele |
| Complications | Vision loss, neurological complications |
| Onset | Congenital |
| Duration | Lifelong |
| Types | |
| Causes | Genetic mutation |
| Risks | |
| Diagnosis | Genetic testing, ophthalmologic examination |
| Differential diagnosis | |
| Prevention | |
| Treatment | Surgical intervention, supportive care |
| Medication | |
| Prognosis | Variable, depending on severity |
| Frequency | Rare |
| Deaths | |
Knobloch syndrome is a rare genetic disorder characterized by a combination of ocular and cranial abnormalities. It is named after the German ophthalmologist Werner Knobloch, who first described the condition. The syndrome is primarily associated with mutations in the COL18A1 gene, which encodes the protein collagen XVIII.
Clinical Features[edit]
Individuals with Knobloch syndrome typically present with a range of symptoms, including:
- Severe myopia (nearsightedness)
- Retinal detachment
- Vitreoretinal degeneration
- Macular degeneration
- Cranial abnormalities, such as occipital encephalocele or microcephaly
- Intellectual disability in some cases
Genetics[edit]
Knobloch syndrome is inherited in an autosomal recessive manner. This means that an individual must inherit two copies of the mutated gene, one from each parent, to manifest the disorder. The primary gene implicated in Knobloch syndrome is COL18A1, which is located on chromosome 21.
Diagnosis[edit]
Diagnosis of Knobloch syndrome is based on clinical evaluation, family history, and genetic testing. Ophthalmologic examination is crucial for identifying the characteristic eye abnormalities. Neuroimaging techniques, such as MRI or CT scan, may be used to detect cranial defects.
Management[edit]
There is no cure for Knobloch syndrome, and treatment is primarily supportive. Management strategies may include:
- Regular ophthalmologic evaluations to monitor and treat eye conditions
- Surgical intervention for retinal detachment
- Special education services for individuals with intellectual disabilities
- Genetic counseling for affected families
Epidemiology[edit]
Knobloch syndrome is extremely rare, with only a few hundred cases reported worldwide. The exact prevalence is unknown due to the rarity of the condition and potential underdiagnosis.
See Also[edit]
References[edit]
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External Links[edit]
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