Pachyonychia congenita: Difference between revisions
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{{SI}} | |||
{{Infobox medical condition | |||
[[File: | | name = Pachyonychia congenita | ||
| image = [[File:Autosomal_dominant_-_en.svg|200px]] | |||
| caption = Pachyonychia congenita is inherited in an [[autosomal dominant]] pattern. | |||
| synonyms = PC | |||
| pronunciation = | |||
| specialty = [[Dermatology]], [[Genetics]] | |||
| symptoms = [[Nail dystrophy]], [[Palmoplantar keratoderma]], [[Oral leukokeratosis]], [[Follicular hyperkeratosis]] | |||
| onset = [[Infancy]] or [[early childhood]] | |||
| duration = [[Lifelong]] | |||
| causes = [[Genetic mutation]] in [[keratin]] genes | |||
| risks = | |||
| diagnosis = [[Clinical diagnosis]], [[genetic testing]] | |||
| differential = [[Other genodermatoses]] | |||
| treatment = [[Symptomatic treatment]], [[pain management]] | |||
| medication = [[Keratolytics]], [[analgesics]] | |||
| frequency = Rare | |||
| deaths = | |||
}} | |||
'''Pachyonychia Congenita''' (PC) is a rare genetic disorder characterized by a variety of skin and nail abnormalities. It is primarily caused by mutations in one of the keratin genes, which are responsible for the structural integrity of epithelial cells. | '''Pachyonychia Congenita''' (PC) is a rare genetic disorder characterized by a variety of skin and nail abnormalities. It is primarily caused by mutations in one of the keratin genes, which are responsible for the structural integrity of epithelial cells. | ||
== Clinical Features == | == Clinical Features == | ||
Pachyonychia Congenita presents with a range of symptoms, which can vary significantly among affected individuals. The most common features include: | Pachyonychia Congenita presents with a range of symptoms, which can vary significantly among affected individuals. The most common features include: | ||
* '''Nail Dystrophy''': Thickened, discolored nails, often with a characteristic "V" shape at the distal edge. | * '''Nail Dystrophy''': Thickened, discolored nails, often with a characteristic "V" shape at the distal edge. | ||
* '''Palmoplantar Keratoderma''': Thickening of the skin on the palms and soles, which can lead to painful blisters and calluses. | * '''Palmoplantar Keratoderma''': Thickening of the skin on the palms and soles, which can lead to painful blisters and calluses. | ||
* '''Oral Leukokeratosis''': White patches on the tongue and inside the mouth. | * '''Oral Leukokeratosis''': White patches on the tongue and inside the mouth. | ||
* '''Follicular Hyperkeratosis''': Rough bumps on the skin, particularly on the elbows, knees, and other extensor surfaces. | * '''Follicular Hyperkeratosis''': Rough bumps on the skin, particularly on the elbows, knees, and other extensor surfaces. | ||
== Genetics == | == Genetics == | ||
Pachyonychia Congenita is inherited in an [[autosomal dominant]] pattern, meaning that a single copy of the mutated gene in each cell is sufficient to cause the disorder. The condition is linked to mutations in one of several keratin genes, including [[KRT6A]], [[KRT6B]], [[KRT6C]], [[KRT16]], and [[KRT17]]. | Pachyonychia Congenita is inherited in an [[autosomal dominant]] pattern, meaning that a single copy of the mutated gene in each cell is sufficient to cause the disorder. The condition is linked to mutations in one of several keratin genes, including [[KRT6A]], [[KRT6B]], [[KRT6C]], [[KRT16]], and [[KRT17]]. | ||
== Diagnosis == | == Diagnosis == | ||
Diagnosis of Pachyonychia Congenita is based on clinical examination and family history. Genetic testing can confirm the diagnosis by identifying mutations in the keratin genes associated with the condition. | Diagnosis of Pachyonychia Congenita is based on clinical examination and family history. Genetic testing can confirm the diagnosis by identifying mutations in the keratin genes associated with the condition. | ||
== Management == | == Management == | ||
There is currently no cure for Pachyonychia Congenita, and treatment focuses on managing symptoms. This may include: | There is currently no cure for Pachyonychia Congenita, and treatment focuses on managing symptoms. This may include: | ||
* '''Pain Management''': Use of analgesics to relieve pain associated with palmoplantar keratoderma. | * '''Pain Management''': Use of analgesics to relieve pain associated with palmoplantar keratoderma. | ||
* '''Foot Care''': Regular trimming of calluses and use of special footwear to reduce pressure on the feet. | * '''Foot Care''': Regular trimming of calluses and use of special footwear to reduce pressure on the feet. | ||
* '''Nail Care''': Regular trimming and care of nails to prevent complications. | * '''Nail Care''': Regular trimming and care of nails to prevent complications. | ||
== See also == | |||
== | |||
* [[Keratin]] | * [[Keratin]] | ||
* [[Genetic disorder]] | * [[Genetic disorder]] | ||
* [[Autosomal dominant]] | * [[Autosomal dominant]] | ||
{{Genetic disorders}} | {{Genetic disorders}} | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Dermatology]] | [[Category:Dermatology]] | ||
Latest revision as of 12:48, 12 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
| Pachyonychia congenita | |
|---|---|
| Synonyms | PC |
| Pronounce | N/A |
| Specialty | Dermatology, Genetics |
| Symptoms | Nail dystrophy, Palmoplantar keratoderma, Oral leukokeratosis, Follicular hyperkeratosis |
| Complications | N/A |
| Onset | Infancy or early childhood |
| Duration | Lifelong |
| Types | N/A |
| Causes | Genetic mutation in keratin genes |
| Risks | |
| Diagnosis | Clinical diagnosis, genetic testing |
| Differential diagnosis | Other genodermatoses |
| Prevention | N/A |
| Treatment | Symptomatic treatment, pain management |
| Medication | Keratolytics, analgesics |
| Prognosis | N/A |
| Frequency | Rare |
| Deaths | |
Pachyonychia Congenita (PC) is a rare genetic disorder characterized by a variety of skin and nail abnormalities. It is primarily caused by mutations in one of the keratin genes, which are responsible for the structural integrity of epithelial cells.
Clinical Features[edit]
Pachyonychia Congenita presents with a range of symptoms, which can vary significantly among affected individuals. The most common features include:
- Nail Dystrophy: Thickened, discolored nails, often with a characteristic "V" shape at the distal edge.
- Palmoplantar Keratoderma: Thickening of the skin on the palms and soles, which can lead to painful blisters and calluses.
- Oral Leukokeratosis: White patches on the tongue and inside the mouth.
- Follicular Hyperkeratosis: Rough bumps on the skin, particularly on the elbows, knees, and other extensor surfaces.
Genetics[edit]
Pachyonychia Congenita is inherited in an autosomal dominant pattern, meaning that a single copy of the mutated gene in each cell is sufficient to cause the disorder. The condition is linked to mutations in one of several keratin genes, including KRT6A, KRT6B, KRT6C, KRT16, and KRT17.
Diagnosis[edit]
Diagnosis of Pachyonychia Congenita is based on clinical examination and family history. Genetic testing can confirm the diagnosis by identifying mutations in the keratin genes associated with the condition.
Management[edit]
There is currently no cure for Pachyonychia Congenita, and treatment focuses on managing symptoms. This may include:
- Pain Management: Use of analgesics to relieve pain associated with palmoplantar keratoderma.
- Foot Care: Regular trimming of calluses and use of special footwear to reduce pressure on the feet.
- Nail Care: Regular trimming and care of nails to prevent complications.
See also[edit]
| Genetic disorders relating to deficiencies of transcription factor or coregulators | ||||||||||||||||||||||||||||||||||
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