Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of dohi): First report from Iran
Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant genodermatosis, presenting in infancy or early childhood with areas of hyperpigmentation on dorsa of hands and feet. DSH has been reported mainly from Japan and only limited cases have been reported from other countries. This i...
Saved in:
Main Authors: | Barzegari Massoumeh (Author), Kiavash Katrin (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2009-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Reticulate acropigmentation of dohi: Dermatoscopic features in two cases
by: Jinal Jainendra, et al.
Published: (2022) -
Dyschromatosis Symmetrica Hereditaria of Late Onset?
by: Caroline Balvedi Gaiewski, et al.
Published: (2014) -
Reticulate acropigmentation of dohi: A case report with insight into genodermatoses with mottled pigmentation
by: Deepak Mohana, et al.
Published: (2012) -
Dyschromatosis symmetrica hereditaria: A retrospective case series and literature review
by: Amy Chia-Ying Peng, et al.
Published: (2013) -
A Case Report of Dyschromatosis Symmetrica Hereditaria with Glucose-6-Phosphate Dehydrogenase Deficiency
by: Wang P, et al.
Published: (2023)