Dyschromatosis universalis: Two cases;Dyschromatose universelle: 2 Cas

Annales de Dermatologie et de Venereologie

Volumn 128, Issue 2, 2001, Pages 136-138

  Dhaoui, M A ^a   Doss, N ^a  

^a MILITARY HOSPITAL OF TUNIS   (Tunisia)

Author keywords

[No Author keywords available]

Indexed keywords

MELANIN;

ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; GENODERMATOSIS; HISTOPATHOLOGY; HUMAN; LEUKOMELANODERMA; MALE; MELANOGENESIS;

ADULT; BIOPSY; DISEASE PROGRESSION; GENES, DOMINANT; HUMANS; HYPERPIGMENTATION; HYPOPIGMENTATION; MALE; MELANINS; MELANOCYTES; PEDIGREE; SKIN DISEASES, GENETIC; ULTRAVIOLET RAYS;

EID: 0035107492     PISSN: 01519638     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (18)

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4. Dyschromatosis: Its occurrence in two indian families with unusual features
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7. Dyschromatosis universalis herediteria an electron microscopic examination
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9. Dyschromatose universelle: Une observation familiale
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18. A case of xeroderma pigmentosum with clinical appearance of dyschromatosis symetrica herediteria