A Rare Case: Touraine Solente Gole Syndrome
نویسندگان
چکیده
منابع مشابه
[Pachydermoperiostosis (Touraine-Solente-Gole syndrome)].
We report on a 38-year-old male patient suffering from pachydermoperiostosis (Touraine-Solente-Golé Syndrome), who underwent a cosmetic operation without success.
متن کاملTouraine-Solente-Gole syndrome in two siblings.
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 int...
متن کامل[Pachydermoperiostosis (Touraine-Solente-Golé syndrome). Case report].
Pachydermoperiostosis or primary hypertrophic osteoarthropathy, also known as Touraine-Solente-Golé syndrome, is a rare process, frequently inherited. In its complete form it is characterized by pachydermia (thickening of the skin), skeletal changes (periostosis) and acropachia (digital clubbing). We report a patient that consulted for skeletal symptoms, as the acropachia and cutaneous manifest...
متن کاملChrist Siemens Touraine syndrome: a case report
BACKGROUND The ectodermal dysplasias are a large and complex group of diseases. CASE PRESENTATION This article presents a case in a 37 years old female patient, referred to the dental clinic for impairment patients maintained by the University of Pernambuco. She presented typical characteristics of Christ Siemens Touraine syndrome such as alterations of the inferior members, a great number of...
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ژورنال
عنوان ژورنال: Haseki Tıp Bülteni
سال: 2017
ISSN: 1302-0072
DOI: 10.4274/haseki.3224