A rare type of primary cutaneous amyloidosis: amyloidosis cutis dyschromica

Author:

Madarasingha N. P.,Satgurunathan K.,De Silva M. V. C.

Publisher

Wiley

Subject

Dermatology

Reference8 articles.

1. Diffuse primary cutaneous amyloidosis;Bourke;Brit J Derm,1992

2. Familial primary cutaneous amyloidosis in a South African family;Hartshone;Clin Exp Dermatol,1999

3. Amyloidosis cutis dyschromica in two siblings;Vijaikumar;Clin Exp Dermatol,2001

4. A clinical variety of localized cutaneous amyloidosis characterized by dyschromia (amyloidosis cutis dyschromica);Morishima;Jpn J Dermatol,1970

5. Familial amyloidosis cutis dyschromica: six cases from three families;Choonhakarn;J Dermatol,2002

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1. Case Report: Amyloidosis Cutis Dyschromica: Dermoscopy and Reflectance Confocal Microscopy and Gene Mutation Analysis of a Chinese Pedigree;Frontiers in Medicine;2021-12-01

2. A Case of Amyloidosis Cutis Dyschromica;E3S Web of Conferences;2021

3. Hyperpigmentary Disorders;Atlas of Dermatoses in Pigmented Skin;2020-12-24

4. Dyschromatosis;Harper's Textbook of Pediatric Dermatology;2019-11-20

5. Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders;Dermatology Research and Practice;2017

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