<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>35(9)</volume><submitter>Manara R</submitter><pubmed_abstract>&lt;h4>Background and purpose&lt;/h4>Kallmann syndrome is a rare inherited disorder due to defective intrauterine migration of olfactory axons and gonadotropin-releasing hormone neurons, leading to rhinencephalon hypoplasia and hypogonadotropic hypogonadism. Concomitant brain developmental abnormalities have been described. Our aim was to investigate Kallmann syndrome-related brain changes with conventional and novel quantitative MR imaging analyses.&lt;h4>Materials and methods&lt;/h4>Forty-five male patients with Kallmann syndrome (mean age, 30.7 years; range, 9-55 years) and 23 age-matched male controls underwent brain MR imaging. The MR imaging study protocol included 3D-T1, FLAIR, and diffusion tensor imaging (32 noncollinear gradient-encoding directions; b-value=800 s/mm2). Voxel-based morphometr</pubmed_abstract><journal>AJNR. American journal of neuroradiology</journal><pagination>1700-6</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7966280</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Brain changes in Kallmann syndrome.</pubmed_title><pmcid>PMC7966280</pmcid><pubmed_authors>Elefante A</pubmed_authors><pubmed_authors>Kallmann Syndrome Neuroradiological Study Group</pubmed_authors><pubmed_authors>Ottaviano G</pubmed_authors><pubmed_authors>Rizzati S</pubmed_authors><pubmed_authors>Rossato M</pubmed_authors><pubmed_authors>Di Salle F</pubmed_authors><pubmed_authors>Salvalaggio A</pubmed_authors><pubmed_authors>Bonanni G</pubmed_authors><pubmed_authors>Cantone E</pubmed_authors><pubmed_authors>Briani C</pubmed_authors><pubmed_authors>Coppola G</pubmed_authors><pubmed_authors>Manara R</pubmed_authors><pubmed_authors>D'Errico A</pubmed_authors><pubmed_authors>Napoli E</pubmed_authors><pubmed_authors>Favaro A</pubmed_authors><pubmed_authors>Sinisi AA</pubmed_authors><pubmed_authors>De Carlo E</pubmed_authors><pubmed_authors>Palumbo V</pubmed_authors><pubmed_authors>Greggio NA</pubmed_authors><pubmed_authors>D'Agosto G</pubmed_authors><pubmed_authors>Citton V</pubmed_authors><pubmed_authors>Brunetti A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Brain changes in Kallmann syndrome.</name><description>&lt;h4>Background and purpose&lt;/h4>Kallmann syndrome is a rare inherited disorder due to defective intrauterine migration of olfactory axons and gonadotropin-releasing hormone neurons, leading to rhinencephalon hypoplasia and hypogonadotropic hypogonadism. Concomitant brain developmental abnormalities have been described. Our aim was to investigate Kallmann syndrome-related brain changes with conventional and novel quantitative MR imaging analyses.&lt;h4>Materials and methods&lt;/h4>Forty-five male patients with Kallmann syndrome (mean age, 30.7 years; range, 9-55 years) and 23 age-matched male controls underwent brain MR imaging. The MR imaging study protocol included 3D-T1, FLAIR, and diffusion tensor imaging (32 noncollinear gradient-encoding directions; b-value=800 s/mm2). Voxel-based morphometr</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Sep</publication><modification>2025-04-18T17:40:56.75Z</modification><creation>2025-04-07T05:17:46.068Z</creation></dates><accession>S-EPMC7966280</accession><cross_references><pubmed>24788131</pubmed><doi>10.3174/ajnr.a3946</doi><doi>10.3174/ajnr.A3946</doi></cross_references></HashMap>