scholarly journals Trichorhinophalangeal Syndrome Type 1: Unusual Case Report and Review of Literature

2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Andrade Rodrigo Soares de ◽  
Gonçalves Juliana de Lima ◽  
Fonseca Cláudia de Alvarenga Diniz ◽  
Taburini Adriana Boeri Freire ◽  
Gomes Heloisa de Sousa ◽  
...  
2018 ◽  
Vol 44 (1) ◽  
Author(s):  
Giulia Trippella ◽  
Paolo Lionetti ◽  
Sara Naldini ◽  
Francesca Peluso ◽  
Matteo Della Monica ◽  
...  

2012 ◽  
Vol 3 (2) ◽  
pp. 209 ◽  
Author(s):  
Ramesh Candamourty ◽  
Suresh Venkatachalam ◽  
B Karthikeyan ◽  
MR Ramesh Babu

2019 ◽  
Vol 121 ◽  
pp. 239-242 ◽  
Author(s):  
Serhat Pusat ◽  
Yahya Cem Erbaş ◽  
Selçuk Göçmen ◽  
Murat Kocaoğlu ◽  
Ersin Erdoğan

2015 ◽  
Vol 14 (3) ◽  
pp. 821-825 ◽  
Author(s):  
Salih Onur Basat ◽  
Ali Rıza Öreroğlu ◽  
Cagdas Orman ◽  
Tolga Aksan ◽  
İlker Üsçetin ◽  
...  

Author(s):  
Gayithri Kulkarni ◽  
Ehtesham Iqbal ◽  
Harish Kulkarni ◽  
Shahanavaj Khaji ◽  
Jyoti Biradar

Author(s):  
B. Thayumanavan ◽  
T. Jeyanthikumari ◽  
P. Meghalapriya

Gorlin-Goltz syndrome is an uncommon autosomal dominant disorder manifesting as a multisystemic disease. Keratocystic odontogenic tumor (KCOT) is considered as the most consistent feature of this syndrome. Dentists play a key role in making early diagnosis of this syndrome. Here we present a case of Gorlin- Goltz syndrome identified by multiple multilocular radiolucencies in the mandible. A review of literature of different diagnostic criteria for Gorlin-Goltz syndrome is also discussed.


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