scholarly journals 507PD Clinical presentation, treatment, outcome, and prognostic factors of non-metastatic Ewing sarcoma family of tumors: A single centre experience of 35 patients

2016 ◽  
Vol 27 ◽  
pp. ix165
Author(s):  
D. Khosla ◽  
A.K. Pandey ◽  
K. Dimri ◽  
S. Garg ◽  
R. Jindal ◽  
...  
2020 ◽  
Vol 31 ◽  
pp. S1252-S1253
Author(s):  
I. Dogan ◽  
E. Aydın ◽  
N. Ak ◽  
K. İbiş ◽  
Ö. Şükrüoğlu ◽  
...  

2012 ◽  
Vol 5 (2) ◽  
pp. 134-140
Author(s):  
Kathrin Strasser-Weippl ◽  
Martin Schreder ◽  
Niklas Zojer ◽  
Heinz Ludwig

2016 ◽  
Vol 44 (7) ◽  
pp. 673-683 ◽  
Author(s):  
T. Billiet ◽  
I. Cleynen ◽  
V. Ballet ◽  
M. Ferrante ◽  
G. Van Assche ◽  
...  

2012 ◽  
Vol 13 (2) ◽  
pp. 60-64
Author(s):  
Bala Basak Oven Ustaalioglu ◽  
Ahmet Bilici ◽  
Mesut Seker ◽  
Taflan Salepci ◽  
Recep Ustaalioglu ◽  
...  

Author(s):  
Sarar Mohamed ◽  
Edna F. Roche ◽  
Hilary M.C.V. Hoey

AbstractAge at diagnosis of girls with Turner syndrome (TS) is an important indicator of successful management. We determined the age, initial clinical presentation, and chromosomal abnormalities in patients with TS.This was a retrospective evaluation of the clinical and laboratory records of patients with TS.Sixty-five patients with TS were identified; 40 (62%) were diagnosed after age 5 years. The main presenting features were short stature, delayed puberty, dysmorphic features, and neonatal lymphoedema. Chromosomal analysis of this cohort showed that 31 patients demonstrated mosaicism, while a 45,X karyotype was observed in 19. The remaining patients had variable abnormalities including deletion, translocation, isochromosome, and ring chromosome. Y-chromosome material was found in four cases.Most patients with TS were diagnosed after age 5 years, had a varied clinical presentation, and had a wide range of chromosomal abnormalities.


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