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International Journal of Advances In Case Reports

Volume 11, Issue 1, 2024
Mcmed International
International Journal of Advances In Case Reports
Issn
XXX-XXXX (Print), 2349 - 8005 (Online)
Frequency
bi-annual
Email
editorijacr@mcmed.us
Journal Home page
http://mcmed.us/about/ijacr
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Abstract
Title
DYSCHROMATOSIS UNIVERSALIS HEREDITARIA A CASE REPORT
Author
Jayakar Thomas1*, Shrisindhuja T2, Tamilarasi S2, and Manoharan D3
Email
jayakarthomas@gmail.com
keyword
Dyschromatosis universalis hereditaria, Dyschromatosis symmetrica hereditaria, Genodermatosis, Acropigmentation of Dohi.
Abstract
Dyschromatosis universalis hereditaria is an autosomal dominant disorder but it can be transmitted sporadically or by autosomal recessive trait. DUH is a rare genodermatosis with pigmentary changes, consisting of varying sized, intermixed with hypopigmented and hyperpigmented macules that make an overall impression of mottling or reticulate pigmentation. We report a 3 year old boy who is presented with asymptomatic diffuse reticulate hyperpigmentation involving the whole body without involvement of eye.
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