scholarly journals Common SPINK-1 genetic mutations do not predispose to Crohn disease

2017 ◽  
Vol 47 ◽  
pp. 1300-1301
Author(s):  
Nevin ORUÇ ◽  
Çağdaş AKTAN ◽  
Afig BERDELİ ◽  
Ahmet Ömer ÖZÜTEMİZ ◽  
Necla OSMAOĞLU
2007 ◽  
Vol 37 (17) ◽  
pp. 5
Author(s):  
ELIZABETH MECHCATIE
Keyword(s):  

2006 ◽  
Vol 44 (08) ◽  
Author(s):  
P Rosenstiel ◽  
D Weichart ◽  
J Gobom ◽  
S Klopfleisch ◽  
R Häsler ◽  
...  

2019 ◽  
Author(s):  
Samantha Anandappa ◽  
Louise Breen ◽  
Ramesh Thurairaja ◽  
Dimitra Christodoulou ◽  
Audrey Jacques ◽  
...  

Consultant ◽  
2020 ◽  
Vol 60 ◽  
Author(s):  
Zachary Field ◽  
Mario Madruga
Keyword(s):  

Author(s):  
Krishna Prasad Lamichhane ◽  
Shaili Pradhan ◽  
Ranjita Shreshta Gorkhali ◽  
Pramod Kumar Koirala

Papillon-Lefèvre syndrome (PLS) is a rare autosomal recessive disorder associated with rapidly progressing periodontitis leading to premature loss of deciduous and permanent dentition and diffuse palmoplantar keratosis. Immunologic alterations, genetic mutations, and role of bacteria are some aetiologic factors. Patients present with early periodontal destruction, so periodontists play a significant role in diagnosis and management. This paper reports a case of Papillon- Lefevre syndrome with its clinical manifestations and challenges for periodontal management which was diagnosed in dental department.


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