Dermatopathia pigmentosa reticularis: Difference between revisions

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{{SI}}
{{Infobox medical condition
| name            = Dermatopathia pigmentosa reticularis
| image          = [[File:Autosomal_dominant_-_en.svg|200px]]
| image_size      = 200px
| alt            =
| caption        = Dermatopathia pigmentosa reticularis is inherited in an [[autosomal dominant]] pattern.
| synonyms        =
| pronounce      =
| specialty      = [[Dermatology]], [[Genetics]]
| symptoms        = [[Reticulate pigmentation]], [[alopecia]], [[nail dystrophy]]
| onset          =
| duration        =
| types          =
| causes          = Mutations in the [[KRT14]] gene
| risks          =
| diagnosis      = [[Clinical diagnosis]], [[genetic testing]]
| differential    =
| prevention      =
| treatment      = [[Symptomatic treatment]]
| medication      =
| prognosis      =
| frequency      = Rare
| deaths          =
}}
'''Dermatopathia pigmentosa reticularis''' is a rare, genetic skin disorder characterized by hyperpigmentation, noncicatricial alopecia, and nail dystrophy. It is a form of [[Ectodermal dysplasia]], a group of conditions which primarily affect the skin, hair, nails, sweat glands, and teeth.
'''Dermatopathia pigmentosa reticularis''' is a rare, genetic skin disorder characterized by hyperpigmentation, noncicatricial alopecia, and nail dystrophy. It is a form of [[Ectodermal dysplasia]], a group of conditions which primarily affect the skin, hair, nails, sweat glands, and teeth.
== Symptoms ==
== Symptoms ==
The primary symptoms of Dermatopathia pigmentosa reticularis include:
The primary symptoms of Dermatopathia pigmentosa reticularis include:
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* [[Noncicatricial alopecia]]: This refers to hair loss that does not lead to scarring.
* [[Noncicatricial alopecia]]: This refers to hair loss that does not lead to scarring.
* [[Nail dystrophy]]: This is a condition characterized by the presence of abnormally shaped or sized nails.
* [[Nail dystrophy]]: This is a condition characterized by the presence of abnormally shaped or sized nails.
== Causes ==
== Causes ==
Dermatopathia pigmentosa reticularis is caused by mutations in the [[KRT14]] gene. This gene provides instructions for making a protein that is a crucial component of [[keratin]] intermediate filaments, which provide strength and resilience to skin cells.
Dermatopathia pigmentosa reticularis is caused by mutations in the [[KRT14]] gene. This gene provides instructions for making a protein that is a crucial component of [[keratin]] intermediate filaments, which provide strength and resilience to skin cells.
== Diagnosis ==
== Diagnosis ==
Diagnosis of Dermatopathia pigmentosa reticularis is based on the clinical symptoms and confirmed by genetic testing. The testing can identify mutations in the KRT14 gene.
Diagnosis of Dermatopathia pigmentosa reticularis is based on the clinical symptoms and confirmed by genetic testing. The testing can identify mutations in the KRT14 gene.
== Treatment ==
== Treatment ==
There is currently no cure for Dermatopathia pigmentosa reticularis. Treatment is symptomatic and supportive, focusing on managing the individual symptoms and complications.
There is currently no cure for Dermatopathia pigmentosa reticularis. Treatment is symptomatic and supportive, focusing on managing the individual symptoms and complications.
== See also ==
== See also ==
* [[Ectodermal dysplasia]]
* [[Ectodermal dysplasia]]
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* [[Noncicatricial alopecia]]
* [[Noncicatricial alopecia]]
* [[Nail dystrophy]]
* [[Nail dystrophy]]
== References ==
== References ==
<references />
<references />
[[Category:Skin conditions]]
[[Category:Skin conditions]]
[[Category:Genetic disorders]]
[[Category:Genetic disorders]]
[[Category:Rare diseases]]
[[Category:Rare diseases]]
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Latest revision as of 18:10, 5 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

Dermatopathia pigmentosa reticularis
Synonyms
Pronounce
Specialty Dermatology, Genetics
Symptoms Reticulate pigmentation, alopecia, nail dystrophy
Complications N/A
Onset
Duration
Types
Causes Mutations in the KRT14 gene
Risks
Diagnosis Clinical diagnosis, genetic testing
Differential diagnosis
Prevention
Treatment Symptomatic treatment
Medication
Prognosis
Frequency Rare
Deaths


Dermatopathia pigmentosa reticularis is a rare, genetic skin disorder characterized by hyperpigmentation, noncicatricial alopecia, and nail dystrophy. It is a form of Ectodermal dysplasia, a group of conditions which primarily affect the skin, hair, nails, sweat glands, and teeth.

Symptoms[edit]

The primary symptoms of Dermatopathia pigmentosa reticularis include:

  • Hyperpigmentation: This is a condition where patches of skin become darker in color than the normal surrounding skin.
  • Noncicatricial alopecia: This refers to hair loss that does not lead to scarring.
  • Nail dystrophy: This is a condition characterized by the presence of abnormally shaped or sized nails.

Causes[edit]

Dermatopathia pigmentosa reticularis is caused by mutations in the KRT14 gene. This gene provides instructions for making a protein that is a crucial component of keratin intermediate filaments, which provide strength and resilience to skin cells.

Diagnosis[edit]

Diagnosis of Dermatopathia pigmentosa reticularis is based on the clinical symptoms and confirmed by genetic testing. The testing can identify mutations in the KRT14 gene.

Treatment[edit]

There is currently no cure for Dermatopathia pigmentosa reticularis. Treatment is symptomatic and supportive, focusing on managing the individual symptoms and complications.

See also[edit]

References[edit]

<references />

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