Rothmund‐Thomson Syndrome in Fraternal Twins
- 28 June 1995
- journal article
- case report
- Published by Wiley in Pediatric Dermatology
- Vol. 12 (2) , 134-137
- https://doi.org/10.1111/j.1525-1470.1995.tb00139.x
Abstract
Fraternal twins of Malay descent had the Rothmund-Thomson syndrome. This is a rare, autosomal recessive disorder characterized by photosensitivity, poikiloderma, short stature, skeletal defects, and juvenile cataracts. This is the first case report of the syndrome from southeast Asia.Keywords
This publication has 13 references indexed in Scilit:
- A case of Rothmund-Thomson syndrome with reduced DNA repair capacityArchives of Dermatology, 1993
- Rothmund-Thomson syndrome with osteosarcomaJournal of the American Academy of Dermatology, 1993
- Rothmund-Thomson syndrome: Review of the world literatureJournal of the American Academy of Dermatology, 1992
- Rothmund-Thomson syndrome: a report of two patients and a review of the literatureBritish Journal of Dermatology, 1990
- Epidermal dysplasia and skeletal deformity in congenital poikiloderma (Rothmund-Thomson syndrome)British Journal of Dermatology, 1987
- Rothmund-Thomson syndrome and malignant diseaseClinical and Experimental Dermatology, 1982
- Premature Multiple Bowen’s Disease in Poikiloderma congenitale with Warty HyperkeratosesDermatology, 1979
- Dental anomalies in the Rothmund-Thomson syndrome: Report of a caseOral Surgery, Oral Medicine, Oral Pathology, 1976
- POIKILODERMA CONGEXITALEBritish Journal of Dermatology, 1936