| Literature DB >> 25628322 |
Ramakrishna Narayanan1, Srinivasa Chennareddy2.
Abstract
Trichorhinophalangeal syndrome type 1 is a rare skeletal dysplasia of autosomal-dominant inheritance due to defects in the TRPS-1 gene. The syndrome is characterised by sparse slow-growing hair, a bulbous pear-shaped nose, cone-shaped epiphyses and deformities of the interphalangeal joints resembling those in rheumatoid arthritis. We present a case of trichorhinophalangeal syndrome in a 23-year-old man who presented with symmetrical painless progressive deformity of the fingers in both hands. 2015 BMJ Publishing Group Ltd.Entities:
Mesh:
Year: 2015 PMID: 25628322 PMCID: PMC4322285 DOI: 10.1136/bcr-2014-207645
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X