Prevalence and natural history of sporadic non-tuberous sclerosis associated renal angiomyolipoma

Author(s):  
A Fittschen ◽  
A Akinli ◽  
W Kratzer ◽  
S Oeztuerk ◽  
MM Haenle ◽  
...  
2017 ◽  
Vol 33 (7) ◽  
pp. 1277-1282 ◽  
Author(s):  
Xue Song ◽  
Zhimei Liu ◽  
Katherine Cappell ◽  
Christopher Gregory ◽  
Qayyim Said ◽  
...  

2014 ◽  
Vol 17 (3) ◽  
pp. A56 ◽  
Author(s):  
K.A. Cappell ◽  
X. Song ◽  
Z. Liu ◽  
E. Eynullayeva ◽  
C. Gregory ◽  
...  

Author(s):  
Fabiano Di Marco ◽  
Silvia Terraneo ◽  
Olívia Olívia Meira Dias ◽  
Gianluca Imeri ◽  
Stefano Centanni ◽  
...  

2018 ◽  
Vol 29 (3) ◽  
pp. 295-301 ◽  
Author(s):  
Denise L. Chan ◽  
Tessa Calder ◽  
John A. Lawson ◽  
David Mowat ◽  
Sean E. Kennedy

AbstractTuberous sclerosis complex (TSC) is an auto-somal-dominant inherited condition with an incidence of approximately 1:6000 births, characterised by deregulated mTOR activity with multi-site hamartomas. Subependymal giant cell astrocytomas (SEGA) are one such hamartoma, affecting up to 24% of patients with TSC. Their intraventricular location may lead to life-threatening obstructive hydrocephalus. Current management is hampered by a lack of understanding regarding the natural history, behaviour and growth patterns of SEGA. We review the current literature to summarise what is known about SEGA in the following areas: (1) diagnostic criteria, (2) prevalence, (3) origin, (4) imaging characteristics, (5) growth rate, (6) genotype-phenotype correlation, (7) congenital SEGA and (8) SEGA as a marker of severity of other TSC manifestations.


1993 ◽  
Vol 150 (6) ◽  
pp. 1782-1786 ◽  
Author(s):  
Mitchell S. Steiner ◽  
Stanford M. Goldman ◽  
Elliot K. Fishman ◽  
Fray F. Marshall

Epilepsia ◽  
2009 ◽  
Vol 51 (7) ◽  
pp. 1236-1241 ◽  
Author(s):  
Catherine J. Chu-Shore ◽  
Philippe Major ◽  
Susana Camposano ◽  
David Muzykewicz ◽  
Elizabeth A. Thiele

Author(s):  
Gregory J. Nason ◽  
Jonathan Morris ◽  
Jaimin R. Bhatt ◽  
Patrick O. Richard ◽  
Lisa Martin ◽  
...  

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