hanhart syndrome
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Familial Richner‐Hanhart syndrome: Report of a sibling with incomplete presentation

2020 ◽  
Vol 33 (6) ◽  
Author(s):  
Fariba Ghalamkarpour ◽  
Nasim Niknezhad ◽  
Nakisa Niknejad
Keyword(s):  
Hanhart Syndrome ◽  
Syndrome Report

scholarly journals HANHART SYNDROME: A RARE CASE REPORT AND REVIEW OF LITERATURE

2019 ◽  
Vol 5 (1) ◽  
pp. 53-55
Author(s):  
Shreya Das . ◽  
Anjana Mazumdar . ◽  
Bikash Chandra Maity . ◽  
Sandip Ghose .
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Review Of Literature ◽  
Rare Case Report ◽  
Hanhart Syndrome

scholarly journals Hanhart syndrome: hypoglossia-hypodactylia syndrome

2019 ◽  
Vol 32 ◽  
Author(s):  
Ipek Guney Varal ◽  
Pelin Dogan
Keyword(s):  
Hanhart Syndrome

Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome

2016 ◽  
Vol 40 (3) ◽  
pp. 461-462 ◽  
Author(s):  
Diogo C. Soares ◽  
Mariana N. Stroparo ◽  
Yu C. Lian ◽  
Cristina Y. Takakura ◽  
Sabrina Wolf ◽  
...  
Keyword(s):  
Warning Signs ◽  
Palmoplantar Hyperkeratosis ◽  
Hanhart Syndrome

Hanhart Syndrome

2014 ◽  
pp. 168-169
Author(s):  
Stefan Mundlos ◽  
Denise Horn
Keyword(s):  
Hanhart Syndrome

scholarly journals Richner-Hanhart Syndrome: A case report of an 11 month old female

2013 ◽  
Vol 42 (4) ◽  
pp. 224
Author(s):  
Biplab Maji ◽  
Sandipan Dhar ◽  
Apurba Ghosh ◽  
Surupa Basu
Keyword(s):  
Case Report ◽  
Hanhart Syndrome

Modification of Mandibular Advancement Osteotomy in a Patient With Hanhart Syndrome

2013 ◽  
Vol 24 (6) ◽  
pp. 2162-2166 ◽  
Author(s):  
Kemal Uğurlu ◽  
Kamuran Zeynep Sevim ◽  
Arzu Akcal ◽  
Semra Karsidag
Keyword(s):  
Mandibular Advancement ◽  
Hanhart Syndrome

Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner–Hanhart Syndrome

Gene ◽  
2013 ◽  
Vol 529 (1) ◽  
pp. 45-49 ◽  
Author(s):  
Yosra Bouyacoub ◽  
Hela Zribi ◽  
Hatem Azzouz ◽  
Fehmi Nasrallah ◽  
Rim Ben Abdelaziz ◽  
...  
Keyword(s):  
Recurrent Mutations ◽  
Hanhart Syndrome
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