A Case of Dyschromatosis Universalis Hereditaria with Chronic Kidney Disease
Keywords:
Dyschromatosis, Dyschromatosis Universalis Hereditaria, dyspigmentation, end stage renal disease, renal failure
Abstract
Dyschromatosis universalis hereditary (DUH) is a rare autosomal dominant inherited dermatosis, although
in some cases autosomal recessive inheritance was reported, which usually appears during childhood and
is characterized by dyspigmentation, with both hyperpigmented and hypopigmented macules. We report a
case of DUH with unexplained adult onset renal failure. The association between DUH and renal failure is yet
to be proven by further studies.
References
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8. Kenani N, Ghariani N, Denguezli M, Sriha B, Belajouza C, Nouira R. Dyschromatosis universalis hereditaria: Two cases. Dermatol Online J. 2008;14:16.
9. Yadalla HK, Pinninti S, Babu AR. Dyschromatosis universalis hereditaria: Infrequent genodermatoses in India. Indian J Hum Genet 2013;19:487-90.
10. Rai R, Kaur I, Handa S, Kumar B. Dyschromatosis universalis hereditaria. Indian J Dermatol Venereol Leprol 2000;66:158- 9.
11. Kenani N, Ghariani N, Denguezli M, Sriha B, Belajouza C, Nouira R. Dyschromatosis universalis hereditaria: Two cases. Dermatol Online J 2008;14:16.
2. Toyama I. Dyschromatosis symmetrica herediteria. Jpn J Dermatol. 1929;29:95–6.
3. Al Hawsawi K, Al Aboud K, Ramesh V, Al Aboud D. Dyschromatosis universalis hereditaria: Report of a case and review of the literature. Pediatr Dermatol. 2002;19:523–6.
4. Bukhari IA, El-Harith EA, Stuhrmann M. Dyschromatosis universalis hereditaria as an autosomal recessive disease in ive members of one family. J Eur Acad Dermatol Venereol.
2006;20:628–9
5. Merino de Paz N, Rodríguez-Martin M, Contreras Ferrer P, Pestana-Eliche M, Martin-Herrera A, Noda-Cabrera A. Photoletter to the editor: Dyschromatosis universalis hereditaria: An infrequently occurring entity in Europe. J
Dermatol Case Rep. 2012;3:96–7.
6. Rai R, Kaur I, Handa S, Kumar B. Dyschromatosis universalis hereditaria. Indian J Dermatol Venereol Leprol. 2000;66:158– 9.
7. Naik CL, Singh G, Rajashekar TS, Okade R. Dyschromatosis universalis hereditaria. Indian J Dermatol. 2009;54:74–5.
8. Kenani N, Ghariani N, Denguezli M, Sriha B, Belajouza C, Nouira R. Dyschromatosis universalis hereditaria: Two cases. Dermatol Online J. 2008;14:16.
9. Yadalla HK, Pinninti S, Babu AR. Dyschromatosis universalis hereditaria: Infrequent genodermatoses in India. Indian J Hum Genet 2013;19:487-90.
10. Rai R, Kaur I, Handa S, Kumar B. Dyschromatosis universalis hereditaria. Indian J Dermatol Venereol Leprol 2000;66:158- 9.
11. Kenani N, Ghariani N, Denguezli M, Sriha B, Belajouza C, Nouira R. Dyschromatosis universalis hereditaria: Two cases. Dermatol Online J 2008;14:16.
Published
2019-11-25
How to Cite
Sakshi, A. kumar dadarwal,Dr. M. K. , D. V. S. , D. M. S. , D. H. T. (2019). A Case of Dyschromatosis Universalis Hereditaria with Chronic Kidney Disease. The Indian Practitioner, 72(11), 21-23. Retrieved from https://articles.theindianpractitioner.com/index.php/tip/article/view/870
Section
Case Reports
