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2014; 60(2):94-96

cm as the irst-line therapy; and LAM patients with mo-

derate to severe lung disease or rapid progression.

2,3

The-

re are certainly other situations where speciic clinical as-

pects of SEGA, angiomyolipoma or LAM patients may

confer high surgical risks. Therefore, the risks of both,

novel or more conventional therapeutic alternatives should

be discussed with the family before making a decision.

Acknowledgements:

LAH is grateful to Steve Ro-

berds and Katie Smith (Tuberous Sclerosis Alliance, Sil-

ver Spring, MD) for discussion and advices on TSC infor-

mation outreach.

R

EFERENCES

1. Northrup H, Krueger DA, on behalf of the International Tuberous Sclerosis

Complex Consensus Group. Tuberous Sclerosis Complex Diagnostic Criteria

Update: Recommendations of the 2012 International Tuberous Sclerosis

Complex Consensus Conference.

Pediatr Neurol

2013; 49: 243-254.

2. Krueger DA, Northrup H, on behalf of the International Tuberous Sclerosis

Complex Consensus Group. Tuberous Sclerosis Complex Surveillance and

Management: Recommendations of the 2012 International Tuberous

Sclerosis Complex Consensus Conference.

Pediatr Neurol

2013; 49:255-265.

3. Roth J, Roach ES, Bartels U, Jó

ź

wiak S, Koenig MK, Weiner HL, Franz DN,

Wang HZ. Subependymal giant cell astrocytoma: diagnosis, screening, and

treatment. Recommendations from the international tuberous sclerosis

complex consensus conference 2012. Pediatr Neurol. 2013; 49:439-44.

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