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Case Reports
. 2014 Nov:24 Suppl 3:S247-9.

Touraine-Solente-Gole syndrome in two siblings

Aisha Iftikhar  1 , Muhammad Haroon Hamid  1 , Ahsan Waheed Rathore  1
Affiliations
  • PMID: 25518791
Case Reports

Touraine-Solente-Gole syndrome in two siblings

Aisha Iftikhar et al. J Coll Physicians Surg Pak. 2014 Nov.

Abstract

Hypertrophic Osteoarthropathy secondary to various causes is not a common entity but primary hypertrophic osteoarthropathy (also called Touraine-Solente-Gole Syndrome) is an extremely rare genetic disorder. It was first described in 1868 by Friedrich and has premier features of clubbing, periostosis and pachydermia. Based on clinical manifestations Touraine Solente and Gole distinguished it into three forms as complete, incomplete and fruste form. Most of the cases described up till now had onset in late adolescence. This report describes two siblings having symptoms consistent with Touraine-Solente-Gole Syndrome which had onset in early childhood.

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