Guttate hypopigmentation in Darier disease: A rare presentation
Darier disease (DD) is an autosomal dominant genodermatosis attributed to ATP2A2 gene mutation which encodes the sarco/endoplasmic reticulum Ca2+ATPase isoform 2. Due to variable gene expressivity, the clinical manifestations are often atypical and of varied severity. The classical feature of DD is...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2024-01-01
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| Series: | Pigment International |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/pigmentinternational.pigmentinternational_4_22 |
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