1. Volume 3, Issue 3, Pages 169-171 (May 2017)
The 6-year follow-up of a Japanese patient with silent erythropoietic protoporphyria 
Megumi Mizawa, MD, PhD, Teruhiko Makino, MD, PhD, Fumina Furukawa, MD, Ryotaro Torai, MD, Hajime Nakano, MD, PhD, Daisuke Sawamura, MD, PhD, Tadamichi Shimizu, MD, PhD 
JAAD Case Reports 
Volume 3, Issue 3, Pages (May 2017)
DOI: /j.jdcr
Copyright © 2017 American Academy of Dermatology, Inc. Terms and Conditions

2. Fig 1
Fluorocytes and the pedigree of the patient. A, Fluorocytes were observed in the patient. B, The pedigree of the family with EPP. The solid symbols refer to symptomatic individuals. T and C represent wild-type IVS3-48T and IVS3-48C, respectively. M, c.286C>T; WT, wild-type.
JAAD Case Reports 2017 3, DOI: ( /j.jdcr )
Copyright © 2017 American Academy of Dermatology, Inc. Terms and Conditions

3. Fig 2 The clinical course of EPP development.
JAAD Case Reports 2017 3, DOI: ( /j.jdcr )
Copyright © 2017 American Academy of Dermatology, Inc. Terms and Conditions

4. Fig 3
The age at the onset of symptoms of 72 EPP patients reported in Japan.
JAAD Case Reports 2017 3, DOI: ( /j.jdcr )
Copyright © 2017 American Academy of Dermatology, Inc. Terms and Conditions