CASE REPORT OF DYSCHROMATOSIS UNIVERSALIS HEREDITARIA

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AMIRNIA M.; RANJKESH M.R.; BABAEINEZHAD SH.

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES Year:2008 | Volume:30 | Issue:2 Page(s): 141-143

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Information Journal Paper

Title

CASE REPORT OF DYSCHROMATOSIS UNIVERSALIS HEREDITARIA

Author(s)

AMIRNIA M. | RANJKESH M.R. | BABAEINEZHAD SH. | Issue Writer Certificate

Keywords

HEREDITARY DYSCHROMATOSISQ3

ACROPIGMENTATION OF DOHIQ3

RETICULATE PIGMENTED DERMATOSISQ3

Abstract

Our case is an 8 years old boy in whom the skin change was found a week after birth. Initially the involvement was limited to limbs but gradually it involved whole body skin. The skin manifestations are composed of hyper and hypo pigmented patch whit in each other. Pathologic finding was compatible with dyschromatosis universals hereditharia. This disease is a rare pigmentary disorder which is characterized with irregular hyper and hypo pigmented macula and patch in a reticular pattern. Skin manifestation can be limited to limbs or can be diffuse in all body skin. The lesions begin mostly several weeks after birth until 6 year of age.

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APA: Copy

AMIRNIA, M., RANJKESH, M.R., & BABAEINEZHAD, SH.. (2008). CASE REPORT OF DYSCHROMATOSIS UNIVERSALIS HEREDITARIA. MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES, 30(2), 141-143. SID. https://sid.ir/paper/47072/en

Vancouver: Copy

AMIRNIA M., RANJKESH M.R., BABAEINEZHAD SH.. CASE REPORT OF DYSCHROMATOSIS UNIVERSALIS HEREDITARIA. MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2008;30(2):141-143. Available from: https://sid.ir/paper/47072/en

IEEE: Copy

M. AMIRNIA, M.R. RANJKESH, and SH. BABAEINEZHAD, “CASE REPORT OF DYSCHROMATOSIS UNIVERSALIS HEREDITARIA,” MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES, vol. 30, no. 2, pp. 141–143, 2008, [Online]. Available: https://sid.ir/paper/47072/en

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