{Reference Type}: Journal Article
{Title}: Incomplete partition type II in its various manifestations: isolated, in association with EVA, syndromic, and beyond; a multicentre international study.
{Author}: D'Arco F;Kandemirli SG;Dahmoush HM;Alves CAPF;Severino M;Dellepiane F;Robson CD;Lequin MH;Rossi-Espagnet C;O'Brien WT;Nash R;Clement E;Juliano AF;
{Journal}: Neuroradiology
{Volume}: 66
{Issue}: 8
{Year}: 2024 Aug 4
{Factor}: 2.995
{DOI}: 10.1007/s00234-024-03386-z
{Abstract}: <B>OBJECTIVE: </B>Incomplete partition type II (IP-II) is characterized by specific histological features and radiological appearance. It may occur in isolation or in association with an enlarged vestibular aqueduct (EVA). Among those with IP-II and EVA, a subset has a diagnosis of Pendred syndrome. This study aimed to explore the prevalence of isolated IP-II, IP-II with EVA, and cases with a genetic or syndromic basis in our cohort.<BR><B>METHODS: </B>From a large, multicentre database of dysplastic cochleae (446 patients, 892 temporal bones), those with imaging features of IP-II were examined in detail, including whether there was a genetic or syndromic association.<BR><B>RESULTS: </B>A total of 78 patients with IP-II were identified. Among these, 55 patients had bilateral IP-II and EVA (only 12 with typical Mondini triad), 8 with bilateral IP-II and normal VA, 2 with bilateral IP-II and unilateral EVA, and 13 with unilateral IP-II (9 with unilateral EVA). Among the group with bilateral IP-II and bilateral EVA in whom genetic analysis was available, 14 out of 29 (48%) had SLC26A4 mutations and a diagnosis of Pendred syndrome, 1 had a FOXI1 mutation, and a few other genetic abnormalities; none had KCNJ10 pathogenic variants.<BR><B>CONCLUSIONS: </B>Bilateral IP-II-bilateral EVA may be seen in the context of Pendred syndrome (SLC26A4 or FOXI1 mutations) but, in the majority of our cohort, no genetic abnormalities were found, suggesting the possibility of unknown genetic associations. IP-II in isolation (without EVA) is favored to be genetic when bilateral, although the cause is often unknown.