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Thank you for your reply. In some cases, these are not large lesions. Unless I’m misunderstanding, we wouldn’t want to generate and/or trust surface/volume metrics. From your responses, it may be best for now to stick with recon-all. Again, thank you for your replies, Eugenio.
Best,
Marc


From: Iglesias Gonzalez, Juan E. <JIGLESIASGONZALEZ@mgh.harvard.edu>
Date: Friday, November 7, 2025 at 10:54 AM
To: Freesurfer support list <freesurfer@nmr.mgh.harvard.edu>
Subject: [EXTERNAL] [Freesurfer] Re: Recon-all-clinical/SynthSeg Concerns w/ Atrophy

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Dear Marc,
Cheers,
/Eugenio

--

Juan Eugenio Iglesias

http://www.jeiglesias.com

From: Rudolph, Marc D <Marc.Rudolph@advocatehealth.org>
Date: Friday, November 7, 2025 at 10:47 AM
To: freesurfer@nmr.mgh.harvard.edu <freesurfer@nmr.mgh.harvard.edu>
Subject: [Freesurfer] Recon-all-clinical/SynthSeg Concerns w/ Atrophy

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Our group is trying to decide on whether we should move to FS8/clinical recon all indefinitely, however we note some inconsistencies. In some instances, SynthSeg seems to completely ignore the underlying structure and “imputes” tissue. Cortical thickness estimates are overall most different from FS7, as may be expected, however, in some cases volumes (e.g., hippocampus) may also be overestimated.  

We have 1mm isotropic T1s, which I see that recon-all may be "generally more accurate than recon-all-clinical.” We’re looking to take advantage of SynthSeg’s ability to overcome poor data quality/dropout/complex folding etc., but do not want to necessarily “in-paint normal looking tissue.” Can you provide any additional information or guidance on the best path forward? 

Thank you very much for your time and any guidance!

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