A Case of Rothmund-Thomson Syndrome

Byoung Dae Kim, You Chan Kim, Soo Chan Kim

Research output: Contribution to journalArticle

Abstract

Rothmund-Thomson syndrome is a rare autosomal recessive genodermatosis, which is characterized by poikiloderma and photosensitivity with variable features including alopecia, sparse hair, short stature, skeletal abnormalities, juvenile cataracts, and an increased risk of developing skin and bone malignancies. A 19-year-old man presented with poikilodermatous skin change on the whole body since three months old, and accompanied by photosensitivity, alopecia, and brachydactyly. As far as we know, this is the first case report of Rothmund-Thomson syndrome in Korea.

Original languageEnglish
Pages (from-to)1206-1209
Number of pages4
JournalKorean Journal of Dermatology
Volume41
Issue number9
Publication statusPublished - 2003 Sep 1

All Science Journal Classification (ASJC) codes

  • Dermatology

Fingerprint Dive into the research topics of 'A Case of Rothmund-Thomson Syndrome'. Together they form a unique fingerprint.

  • Cite this

    Kim, B. D., Kim, Y. C., & Kim, S. C. (2003). A Case of Rothmund-Thomson Syndrome. Korean Journal of Dermatology, 41(9), 1206-1209.