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Information Journal Paper

Title

CONGENITAL DIFFUSE MELANOSIS IN A FATHER AND TWO SONS

Pages

  177-189

Abstract

CONGENITAL DIFFUSE MELANOSIS is one of the rarest clinical manifestations of hereditary universal melanosis and only few cases have been reported all over the world. The presented case is a 54-year-old man who presented to us complaining of erythematous annular lesions on his face and neck since 8 months ago. Diffuse pigmentation of his skin took our attention. According to the patient, DIFFUSE HYPERPIGMENTATION was present at birth and there was no obvious changes up to now. His mother and sister had similar hyperpigmentation. He had two sons with a similar hyperpigmentaion, but his daugher had normal skin pigmentation. All laboratory investigation causes of for the hyperpigmentaion were reported normal and investigation of secondary for causes hyperpigmentation not reveal any did abnormality. In histopathologic assay, the erythematous lesion was reported to be discoid lupus erythematosus and the diagnosis of lesion reported as hyperpigmented CONGENITAL DIFFUSE MELANOSIS.

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  • Cite

    APA: Copy

    BARZEGARI, M., EMADI, S.N., & ROUBATI, R.M.. (2005). CONGENITAL DIFFUSE MELANOSIS IN A FATHER AND TWO SONS. IRANIAN JOURNAL OF DERMATOLOGY, 8(3), 177-189. SID. https://sid.ir/paper/361178/en

    Vancouver: Copy

    BARZEGARI M., EMADI S.N., ROUBATI R.M.. CONGENITAL DIFFUSE MELANOSIS IN A FATHER AND TWO SONS. IRANIAN JOURNAL OF DERMATOLOGY[Internet]. 2005;8(3):177-189. Available from: https://sid.ir/paper/361178/en

    IEEE: Copy

    M. BARZEGARI, S.N. EMADI, and R.M. ROUBATI, “CONGENITAL DIFFUSE MELANOSIS IN A FATHER AND TWO SONS,” IRANIAN JOURNAL OF DERMATOLOGY, vol. 8, no. 3, pp. 177–189, 2005, [Online]. Available: https://sid.ir/paper/361178/en

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