scholarly journals Cellular Desmoplastic or Anaplastic Supratentorial Ependymoma with Neuronal Differentiation in Probable Associated to RELA Fusion? Case Report

Author(s):  
Tena-Suck Martha Lilia ◽  
Ruiz-Treviño Armando ◽  
Chávez-Macías Laura ◽  
Peñafiel-Salgado Carlos ◽  
Sánchez-Garibay Carlos
2019 ◽  
Vol 14 (2) ◽  
pp. 42-48
Author(s):  
N. G. Lyukshina

Pitt–Hoppkins syndrome is rare genetic disorder caused by a molecular variant of TCF4 which is involved in embryologic neuronal differentiation. The syndrome is characterized by specific facial dysmorphism, phychomotor delay, autistic behavior and intellectual disability. Other associated features include ealy-onset myopia, seizures, constipation and hyperventilation-apneic spells. We introduced a clinical case of the patient with molecularly confirmed TCF4 variant and previously undescribed combination with syndrome of the electrical status epilepticus during sleep.


2017 ◽  
Vol 51 (6) ◽  
pp. 588-593 ◽  
Author(s):  
Seong-Ik Kim ◽  
Yoojin Lee ◽  
Seung Ki Kim ◽  
Hyoung Jin Kang ◽  
Sung-Hye Park

2021 ◽  
Vol 9 (3) ◽  
pp. 221-226
Author(s):  
  Dr. Balaji S ◽  
Dr. Jonathan Arnold ◽  
Dr. Govindaraj T ◽  
Dr. Muthu kumar

2002 ◽  
Vol 42 (9) ◽  
pp. 399-405 ◽  
Author(s):  
Michimasa EBATO ◽  
Akira TSUNODA ◽  
Chikashi MARUKI ◽  
Furitsu IKEYA ◽  
Motoi OKADA

Pulse ◽  
2014 ◽  
Vol 6 (1-2) ◽  
pp. 51-52
Author(s):  
A Khaled ◽  
MA Joarder ◽  
M Chandy ◽  
TA Nasir

Central neurocytoma is a tumour showing neuronal differentiation. This tumour usually located in ventricles occurs at young age and carries favorable prognosis. For this, accurate diagnosis is essential. There is no published case report of central neurocytoma in Bangladesh. With these objectives, we have presented a case report of central neurocytoma in a 37 years old female. DOI: http://dx.doi.org/10.3329/pulse.v6i1-2.20351 Pulse Vol.6 January-December 2013 p.51-52


2021 ◽  
Author(s):  
Jian Wang ◽  
Liang Wang ◽  
Lin Fu ◽  
Qing‐Chang Li ◽  
Xue‐Shan Qiu ◽  
...  

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