Phylloid hypomelanosis: Difference between revisions
CSV import Tags: mobile edit mobile web edit |
CSV import Tags: mobile edit mobile web edit |
||
| Line 31: | Line 31: | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
{{stub}} | {{stub}} | ||
{{No image}} | |||
Revision as of 23:56, 10 February 2025
Phylloid hypomelanosis is a rare skin condition characterized by the presence of leaf-shaped (phylloid) patches of lighter skin (hypomelanosis). The condition is usually present at birth or appears in early childhood. The patches are typically found on the trunk and limbs, and are often symmetrical. The cause of phylloid hypomelanosis is currently unknown.
Symptoms
The primary symptom of phylloid hypomelanosis is the presence of leaf-shaped patches of lighter skin. These patches are typically found on the trunk and limbs, and are often symmetrical. Other symptoms may include:
- Mild itching
- Sensitivity to sun exposure
- Increased risk of skin cancer
Causes
The cause of phylloid hypomelanosis is currently unknown. It is thought to be a genetic condition, but the specific genes involved have not been identified.
Diagnosis
Phylloid hypomelanosis is typically diagnosed based on the characteristic appearance of the skin patches. A skin biopsy may be performed to confirm the diagnosis.
Treatment
There is currently no cure for phylloid hypomelanosis. Treatment is typically focused on managing symptoms and preventing complications. This may include:
- Use of sunscreen to protect the skin from sun exposure
- Regular skin checks to monitor for signs of skin cancer
See also
References
<references />


