scholarly journals Lipomatous Hamartoma

2020 ◽  
Author(s):  
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CHEST Journal ◽  
2018 ◽  
Vol 154 (4) ◽  
pp. 672A
Author(s):  
PRATHIK KRISHNAN ◽  
POORNIMA RAMADAS ◽  
MANJU PAUL


2014 ◽  
Vol 5 (12) ◽  
pp. 1113-1116 ◽  
Author(s):  
Daniele De Falco Alfano ◽  
Marilina Totaro ◽  
Cristina Zagà ◽  
Riccardo Duati ◽  
Andrea Bernardoni ◽  
...  


2018 ◽  
Vol 16 (05) ◽  
pp. 369-378
Author(s):  
Maria Garozzo ◽  
Daniele Attardo ◽  
Pierluigi Smilari ◽  
Filippo Greco ◽  
Agata Fiumara ◽  
...  

AbstractEncephalocraniocutaneous lipomatosis is a sporadic, congenital neurocutaneous disorder characterized by the involvement of skin, central nervous system, and eye. A non-hereditary, autosomal mutation that may survive only in a mosaic state may be the cause of the clinical picture of the syndrome. Less than 80 patients have been so far reported and their clinical manifestations consisted of unilateral lipomatous hamartoma of the scalp or eyelid, epibulbar choristomas, and ipsilateral brain malformations. There is no clinical correlation between the severity of brain malformations and the clinical manifestations, and many patients with extremely extensive cerebral abnormalities are only minimal symptomatic. Seizures and mental retardation may also occur. The natural history is often favorable, without drug-resistant seizures and normal intelligence in most of the cases.



2011 ◽  
Vol 59 (03) ◽  
pp. 188-190
Author(s):  
M. Kim ◽  
K. Lee ◽  
K. Kim ◽  
H.-K. Park ◽  
Y. Kim ◽  
...  
Keyword(s):  


Circulation ◽  
2016 ◽  
Vol 133 (8) ◽  
Author(s):  
Yuta Torii ◽  
Hirotsugu Yamada ◽  
Susumu Matsukuma ◽  
Susumu Nishio ◽  
Kenya Kusunose ◽  
...  


2005 ◽  
Vol 53 (10) ◽  
pp. 577-579 ◽  
Author(s):  
Tomoyuki Wada ◽  
Shinji Miyamoto ◽  
Hirofumi Anai ◽  
Hirofumi Zaizen ◽  
Tetsuo Hadama


2008 ◽  
Vol 14 (3) ◽  
pp. 227-234
Author(s):  
R. H. KOEHL ◽  
G. B. SOLITARE ◽  
R. R. HEFFNER




Cureus ◽  
2019 ◽  
Author(s):  
Jeff D Hodges ◽  
Ray Chihara ◽  
Edward Y Chan ◽  
Min Kim


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