Sporadic Case of dyschromatosis universalis hereditaria showing moderate response to narrow-band ultraviolet-B

Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis where the affected manifests mottled pigmentation with intermingled hyper- and hypo-pigmented macules. On most occasions, the lesions begin on limbs and then extend to trunk. Most of the cases reported in literature are from Japan...

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Main Authors: Sarita Sasidharanpillai (Author), Amal Shyam (Author), Shiny P Manakkad (Author), Ettapurath N Abdul Latheef (Author), Saleem Rahima (Author), Nina Paul (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2019-01-01T00:00:00Z.
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100 1 0 |a Sarita Sasidharanpillai  |e author 
700 1 0 |a Amal Shyam  |e author 
700 1 0 |a Shiny P Manakkad  |e author 
700 1 0 |a Ettapurath N Abdul Latheef  |e author 
700 1 0 |a Saleem Rahima  |e author 
700 1 0 |a Nina Paul  |e author 
245 0 0 |a Sporadic Case of dyschromatosis universalis hereditaria showing moderate response to narrow-band ultraviolet-B 
260 |b Wolters Kluwer Medknow Publications,   |c 2019-01-01T00:00:00Z. 
500 |a 2319-7250 
500 |a 10.4103/ijpd.IJPD_33_18 
520 |a Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis where the affected manifests mottled pigmentation with intermingled hyper- and hypo-pigmented macules. On most occasions, the lesions begin on limbs and then extend to trunk. Most of the cases reported in literature are from Japan. It is rarer in Indians. In this report, we describe a 12-year-old male child with DUH, who showed response to narrow-band ultraviolet-B therapy. 
546 |a EN 
690 |a Child 
690 |a dyschromatosis universalis hereditaria 
690 |a narrow-band ultraviolet-B 
690 |a Dermatology 
690 |a RL1-803 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Indian Journal of Paediatric Dermatology, Vol 20, Iss 2, Pp 172-173 (2019) 
787 0 |n http://www.ijpd.in/article.asp?issn=2319-7250;year=2019;volume=20;issue=2;spage=172;epage=173;aulast=Sasidharanpillai 
787 0 |n https://doaj.org/toc/2319-7250 
856 4 1 |u https://doaj.org/article/e6ec20fb83e949e58fcf4ac9ba8fa9f5  |z Connect to this object online.