The lungs in tuberous sclerosis complex: a case report

2007 ◽  
Vol 56 (2) ◽  
Author(s):  
NC Iheonunekwu ◽  
TM Ibrahim ◽  
BD Crosdale ◽  
RH Gangappa
BMC Neurology ◽  
2020 ◽  
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Author(s):  
Valérie Mongrain ◽  
Nicolaas H. van Doesburg ◽  
Françoise Rypens ◽  
Catherine Fallet-Bianco ◽  
Justine Maassen ◽  
...  

2020 ◽  
Vol 33 ◽  
pp. 101413
Author(s):  
Virgilio Michael Ambrosi Grappelli ◽  
Serena Pastore ◽  
Claudia Fede Spicchiale ◽  
Lorenzo Alteri ◽  
Andrea Turbanti ◽  
...  

2008 ◽  
Vol 121 (10) ◽  
pp. 959-960
Author(s):  
Guo-guang ZHAO ◽  
Yong-zhi SHAN ◽  
Jian-xin DU ◽  
Feng LING

2019 ◽  
Vol 35 (5) ◽  
pp. 426-430
Author(s):  
Bailey Sarff ◽  
Randall Floyd ◽  
Amy Bildner ◽  
Janell Stormo ◽  
Kelsy Fisher

Cardiac rhabdomyomas are the most common fetal cardiac tumor. They can be detected in the second and third trimesters. Rhabdomyomas are most commonly associated with the genetic disorder tuberous sclerosis complex. When associated with tuberous sclerosis complex, cardiac rhabdomyomas usually regress within the first few years of life, without complications. Symptoms depend on the size, number, and location of the rhabdomyomas. A case report of multiple cardiac rhabdomyomas that was found at 35 weeks’ gestation and is discussed.


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