| CASE REPORT |
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| Year : 2013 | Volume
: 18
| Issue : 2 | Page : 137-139 |
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Dyschromatosis universalis hereditaria: A rare case report
Esha Bisne1, Sonia Jain1, VB Shivkumar2
1 Department of Skin and Veneral Diseases, Mahatma Gandhi Institute of Medical Sciences, Sewagram, Wardha, Maharashtra, India
2 Department of Pathology, Mahatma Gandhi Institute of Medical Sciences, Sewagram, Wardha, Maharashtra, India
Correspondence Address:
Esha Bisne
18 Married PG Hostel, Mahatma Gandhi Institute of Medical Sciences Campus, Sewagram, Wardha, Maharashtra
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0971-9903.117794
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Dyschromatosis universalis hereditaria is an autosomal dominant disorder but may be recessive or sporadically inherited disorder, infrequently occurring genodermatosis with peculiar pigmentary changes, consisting of varying sized, intermingled hyperpigmented and hypopigmented macules that give an overall impression of mottling. Herein, we report this extremely rare case of dyschromatosis universalis hereditaria in a young male with a family history of the same disorder in his younger brother. |
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