WERNER SYNDROME: A NEW CASE REPORT

“Werner’s syndrome” or premature aging syndrome is a rare autosomal recessive genetic disease. It is responsible of several complications related to age, including atherosclerosis and association with cancer. We report the case of a 36 year-old-patient, admitted to department of Internal Medic... Ausführliche Beschreibung

1. Person: Faida Ajili verfasserin
Weitere Personen: Wafa Garbouj verfasserin; Najeh Boussetta verfasserin; Janet Laabidi verfasserin; Nadia Ben Abdelhafidh verfasserin; Bassem Louzir verfasserin; Salah Othmani verfasserin
Quelle: In Nasza Dermatologia Online (01.10.2013)
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Format: Online-Artikel
Sprache: English
Spanish
French
Greek, Modern (1453- )
Veröffentlicht: 2013
Beschreibung: Online-Ressource
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  Creative Commons License Source: Directory of Open Access Journals (DOAJ).
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520 |a “Werner’s syndrome” or premature aging syndrome is a rare autosomal recessive genetic disease. It is responsible of several complications related to age, including atherosclerosis and association with cancer. We report the case of a 36 year-old-patient, admitted to department of Internal Medicine of the military hospital of Tunis for suspicion of systemic sclerosis. The patient had all the major signs of Werner syndrome (bilateral cataract, sclerotic skin, “bird face”, baldness, small size, parental consanguinity) and 4 minor signs (type 2 diabetes, hypogonadism, squeaky voice, and flat feet). She has also a brother with the same morphotype died at the age of 32 by a myocardial infarction. The current follow-up time is 9 years.. 
700 0 |a Wafa Garbouj  |e verfasserin  |4 aut 
700 0 |a Najeh Boussetta  |e verfasserin  |4 aut 
700 0 |a Janet Laabidi  |e verfasserin  |4 aut 
700 0 |a Nadia Ben Abdelhafidh  |e verfasserin  |4 aut 
700 0 |a Bassem Louzir  |e verfasserin  |4 aut 
700 0 |a Salah Othmani  |e verfasserin  |4 aut 
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