Literature DB >> 25628322

Crooked fingers and sparse hair: an interesting case of trichorhinophalangeal syndrome type 1.

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.

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Year:  2015        PMID: 25628322      PMCID: PMC4322285          DOI: 10.1136/bcr-2014-207645

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  3 in total

1.  Trichorhinophalangeal syndrome type I: symptoms and signs, radiology and genetics.

Authors:  S Noltorp; U L Kristoffersson; N Mandahl; L Stigsson; B Svensson; C O Werner
Journal:  Ann Rheum Dis       Date:  1986-01       Impact factor: 19.103

2.  The tricho-rhino-phalangeal syndrome. A report of 14 cases in 7 kindreds.

Authors:  C J Howell; R Wynne-Davies
Journal:  J Bone Joint Surg Br       Date:  1986-03

3.  Trichorhinophalangeal Syndrome Type I: A Patient with Two Novel and Different Mutations in the TRPS1 Gene.

Authors:  Catarina Dias; Lara Isidoro; Mafalda Santos; Helena Santos; Jorge Sales Marques
Journal:  Case Rep Genet       Date:  2013-04-17
  3 in total

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