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Dyschromatosis Symmetrica Hereditaria of Late Onset?
Joint Authors
Zuneda Serafini, Sergio
Werner, Betina
Deonizio, Janyana M. D.
Gaiewski, Caroline Balvedi
Source
Case Reports in Dermatological Medicine
Issue
Vol. 2014, Issue 2014 (31 Dec. 2014), pp.1-3, 3 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2014-02-04
Country of Publication
Egypt
No. of Pages
3
Main Subjects
Abstract EN
Dyschromatosis symmetrica hereditaria (DSH), also known as reticulated acropigmentation of Dohi, is an autosomal dominant disease with high penetrance, characterized by hypo- and hyperpigmented macules of varying sizes on the dorsal of the extremities with reticulated pattern.
This paper presents a female patient with typical dermatological lesions, but only diagnosed in adulthood.
It is necessary to perform differential diagnosis with other pigmentary disorders.
This entity is not very common in South America, and the vast majority of cases were described in Japanese population.
Since it is a benign disease, it is important to be aware of this diagnosis in order to establish the correct conduct for these patients.
American Psychological Association (APA)
Gaiewski, Caroline Balvedi& Zuneda Serafini, Sergio& Werner, Betina& Deonizio, Janyana M. D.. 2014. Dyschromatosis Symmetrica Hereditaria of Late Onset?. Case Reports in Dermatological Medicine،Vol. 2014, no. 2014, pp.1-3.
https://search.emarefa.net/detail/BIM-1016975
Modern Language Association (MLA)
Gaiewski, Caroline Balvedi…[et al.]. Dyschromatosis Symmetrica Hereditaria of Late Onset?. Case Reports in Dermatological Medicine No. 2014 (2014), pp.1-3.
https://search.emarefa.net/detail/BIM-1016975
American Medical Association (AMA)
Gaiewski, Caroline Balvedi& Zuneda Serafini, Sergio& Werner, Betina& Deonizio, Janyana M. D.. Dyschromatosis Symmetrica Hereditaria of Late Onset?. Case Reports in Dermatological Medicine. 2014. Vol. 2014, no. 2014, pp.1-3.
https://search.emarefa.net/detail/BIM-1016975
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1016975