A case of Maffucci syndrome with a buccal hemangioma harboring a mutation in IDH1

Oral Oncology ◽  
2021 ◽  
Vol 122 ◽  
pp. 105553
Author(s):  
Norihisa Ichimura ◽  
Noriyuki Yamamoto ◽  
Naoto Toyama ◽  
Hideharu Hibi
Keyword(s):  
Author(s):  
Barry H. Davison ◽  
Joan W. Mayfield
Keyword(s):  

2019 ◽  
Vol 32 (3) ◽  
Author(s):  
Vishal Gupta ◽  
Asit Ranjan Mridha ◽  
Binod K. Khaitan

2021 ◽  
Vol 14 (3) ◽  
pp. e239619
Author(s):  
Gopalkrishna G Verma ◽  
Vijay Kumar Jain ◽  
Karthikeyan P Iyengar

Maffucci syndrome is a rare congenital, non-hereditary condition characterised by presence of multiple enchondromas and haemangiomas. Enchondromatous lesions affecting epiphysial growth plates can lead to angular deformities and leg-length discrepancy in the lower limb. We describe a 12-year-old girl with monomelic Maffucci syndrome affecting her left lower limb. She presented with progressive genu valgus deformity of her left knee. This caused her to limp during her gait and was a cosmetic dissatisfaction. The deformity affected her quality of life. She underwent a supracondylar distal femoral corrective osteotomy with a successful clinical outcome and restoration of her gait and cosmetic deformity.


2018 ◽  
Vol 71 (S1) ◽  
pp. 652-656
Author(s):  
Swathi Velagapudi ◽  
Saad M. Alshammari ◽  
Suresh Velagapudi

Author(s):  
S Fleming ◽  
P Player ◽  
S Ladani ◽  
F Miall ◽  
J Goldney ◽  
...  
Keyword(s):  

Author(s):  
Fernando César Toniazzi Lissa ◽  
Juliana Sonego Argente ◽  
Geórgia Nunes Antunes ◽  
Franciani de Oliveira Basso ◽  
Janara Furtado

2009 ◽  
Vol 23 (4) ◽  
pp. 278-280 ◽  
Author(s):  
Sean Fang ◽  
Donna Dimond ◽  
Rouin Amirfeyz ◽  
Martin Gargan

2019 ◽  
Vol 130 ◽  
pp. e356-e361
Author(s):  
Soliman Oushy ◽  
Maria Peris-Celda ◽  
Jamie J. Van Gompel

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