{"doi":"10.1002/mdc3.70176","title":"“Mini Molar Tooth” Sign in <scp> <i>POLR3B</i> </scp> ‐Associated Cerebellar Ataxia with Hypomyelinating Leukodystrophy","abstract":"In 2003, we reported two ataxic sisters with hypomyelinating leukodystrophy within the spectrum of the cerebello-cerebral-oculo-renal syndrome but with negative genetic workup.1 Two decades later, whole-exome sequencing (WES) revealed pathogenic heterozygous variants in POLR3B. Besides resolving a previously undiagnosed but well characterized disorder, we aim to highlight what we refer to as the “mini molar tooth” sign, originally suggesting a variant of Joubert syndrome. We propose that this imaging sign is a diagnostic clue in POLR3B-related leukodystrophy. Both sisters, first evaluated in their 20s, exhibited developmental delay, ataxia, hypogonadism, and poorly formed secondary teeth. Neurologic examination showed impaired eye abduction, dysarthria, bradylalia, hypoplastic optic nerves, jerky smooth pursuit, slow initiation of saccades, horizontal nystagmus, and appendicular and truncal ataxia. Both had hypoplastic, discolored teeth, and required pharmacologic induction and maintenance of menstruation. No longer progressing after late adolescence, the sisters are now in their late forties (Video 1 and 2). Imaging findings showed absent myelination in the centrum ovale and corpus callosum, anterior commissure, and U-fibers except for a single bundle in one sister.1 The severely hypoplastic cerebellum, leaving behind a remnant of the anterior vermis along with hypoplasia of the superior cerebellar peduncles, yielded a “mini molar tooth” sign, reminiscent of the “molar tooth sign” of Joubert syndrome (Fig. 1, second image). WES analysis of Sister 2 identified two heterozygous pathogenic variants in POLR3B (OMIM614366) [Variant 1: NM_018082.6:c.1568 T>A(p.Val523Glu), pathogenic based on criteria PM2, PP3, PS1; Variant 2: NM_018082.6:c.3082C>T(p.Arg1028Ter), a presumed novel nonsense variant, pathogenic based on criteria PVS1, PM2, PP3]. The first variant has been previously reported; the second variant, not previously documented, is consistent with loss-of-function and meets established pathogenicity criteria. The presence of these two pathogenic variants supports a molecular diagnosis of POLR3B-related leukodystrophy (OMIM614381). The “molar tooth” sign is characterized by cerebellar vermis hypoplasia with enlarged fourth ventricle, increased depth of the interpeduncular fossa, and elongated/reoriented superior cerebellar peduncles. It is a signature feature of Joubert syndrome, which includes intellectual disability, episodic hyperpnea, abnormal eye movements, ataxia, although it can be associated with other syndromes, including Dekaban-Arima, Senior-Löken, COACH (cerebellar vermis hypoplasia, oligophrenia, ataxia, coloboma, hepatic fibrosis).4 Neither Joubert nor any of these other developmental abnormalities exhibit hypomyelination. The difference of the midbrain/vermis configuration with regards to the molar tooth sign on imaging between the POLR3B-ataxia sisters and Joubert syndrome is a thin rather than thick superior cerebellar peduncles and shallower anterior foramen cecum. We propose that this ‘mini molar tooth’ sign be considered an imaging clue for underlying POLR3B mutation. A strikingly similar finding (Fig. 1, third image) was reported in three siblings with onset at 5 years of cerebellar ataxia with cerebral hypomyelination, which may have been the result of a POLR3B mutation (the corresponding author of this publication indicated he no longer can reach these siblings).2 POLR3-related leukodystrophy includes several phenotypes associated with ataxia: hypomyelination, hypodontia, hypogonadotropic hypogonadism (4H syndrome); delayed dentition, and hypomyelination; tremor-ataxia with central hypomyelination; leukodystrophy with oligodontia, and hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum.2, 5 POLR3A encodes the largest subunit of RNA polymerase-III (Pol-III), and POLR3B the second largest Pol-III subunit.6 POLR3A mutations are associated with earlier, more severe clinical and hypo","journal":"Movement Disorders Clinical Practice","year":2025,"id":567943,"datarank":0.0,"base_score":0.0,"endowment":0.0,"self_citation_contribution":0.0,"citation_network_contribution":0.0,"self_endowment_contribution":0.0,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":0,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":0.9459,"is_data_producer":false,"deposit_databanks":null,"is_oa":true,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":"2025-01-01","fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":263852,"name":"Marcelo Kauffman","orcid":"0000-0003-1680-5092","position":1,"is_corresponding":false},{"id":1472460,"name":"Blanca Talavera de la Esperanza","orcid":null,"position":2,"is_corresponding":false},{"id":1472461,"name":"Zhuanzhuan Yu","orcid":null,"position":3,"is_corresponding":false},{"id":106044,"name":"Donald L. Gilbert","orcid":"0000-0002-9245-6878","position":4,"is_corresponding":false},{"id":233015,"name":"Alberto J. Espay","orcid":"0000-0002-3389-136X","position":5,"is_corresponding":false},{"id":373825,"name":"Luca Marsili","orcid":"0000-0002-6438-9911","position":0,"is_corresponding":true}],"reference_count":8,"raw_metadata":null,"created_at":"2026-07-19T02:56:48.183032Z","pmid":"40498034","pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}