C1-C2 instability in a 3-year-old girl with Morquio syndrome: A technically challenging fixation under intra-operative CT scan and neuronavigation

2021 ◽  
Author(s):  
N. Serratrice ◽  
K. Farah ◽  
G. Baucher ◽  
A. Cano ◽  
D. Scavarda ◽  
...  
2018 ◽  
Vol 8 (3) ◽  
pp. 266-269
Author(s):  
AKM Motiur Rahman Bhuiyan ◽  
Maftahul Jannat ◽  
Md Zilan Miah Sarker ◽  
Mohammad Tanvir Islam ◽  
Amit Roy Chowdhury

Morquio syndrome is a rare autosomal recessive disorder of mucopolysaccharide metabolism, also called mucopolysaccharidosis type IV. We report a case of Morquio syndrome in a16-year- old girl of normal intelligence, who got herself admitted in Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh. The patient had short stature and skeletal deformity and she belonged to a non-consanguineous marriage of her parents. She was diagnosed on the basis of clinical features, typical radiological changes and positive urinary mucopolysaccharide screening test.Birdem Med J 2018; 8(3): 266-269


2019 ◽  
Vol 86 (1) ◽  
pp. 123-124
Author(s):  
Stéphane Mitrovic ◽  
Hélène Gouze ◽  
Thierry Schaeverbeke ◽  
Laure Gossec ◽  
Bruno Fautrel

2014 ◽  
Vol 34 (2) ◽  
pp. 223-228 ◽  
Author(s):  
Wagner A.R. Baratela ◽  
Michael B. Bober ◽  
Mihir M. Thacker ◽  
Mohan V. Belthur ◽  
Murat Oto ◽  
...  

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