Comprehensive Clinical, Neuroradiologic, and Oral Health of 23 Individuals With MOPDII
Background and Objectives Microcephalic osteodysplastic primordial dwarfism type II (MOPDII; MIM #210720) is a rare autosomal recessive disorder characterized by severe growth failure and microcephaly, frequently complicated by central nervous system (CNS) anomalies and early-onset cerebrovascular disease. This study aimed to define the neurologic, radiologic, molecular, and oral-dental features of a MOPDII cohort, with particular emphasis on cerebrovascular involvement, and to assess genotype-phenotype correlations. Methods Molecular diagnosis was established using next-generation sequencing, including targeted gene panel sequencing (n = 11) and exome sequencing (n = 1), or Sanger sequencing (n = 11). Clinical data, neuroimaging and vascular findings, systematic oral-dental examinations, and molecular results were retrospectively reviewed. Results Twenty-three patients from 18 unrelated consanguineous families were included. Seventeen distinct homozygous PCNT variants were identified, including 5 splice-site, 5 frameshift, and 7 nonsense variants; of these, 12 were novel. Structural CNS anomalies were common, with the thin corpus callosum being the most frequent finding, observed in 14 of 17 patients (82%) who underwent cranial imaging. Moyamoya disease was identified in 12 patients (70.5%), of whom 7 experienced chronic or acute cerebral infarctions and/or intracranial hemorrhage. Three patients with moyamoya disease died of complications related to vascular involvement. The 2 oldest patients developed severe peripheral arterial and coronary artery occlusions, leading to spontaneous limb amputation and acute myocardial infarction. Oral-dental evaluation, performed in 14 patients (61%), revealed microdontia, malformed teeth, and root shortening. No consistent genotype-phenotype correlation was identified for cerebrovascular or orodental manifestations. Discussion MOPDII is strongly associated with moyamoya disease and represents a major cause of neurologic morbidity and mortality. Early and longitudinal neuroimaging, including brain MRI and angiographic assessment, should be integral to patient management. Oral-dental abnormalities are common and merit routine evaluation.
Authors
- İsmet Rezani Toptancı (ORCID: https://orcid.org/0000-0003-2298-9617)
- Nagihan Koç (ORCID: https://orcid.org/0000-0002-3339-7783)
- Pelin Özlem Şimşek‐Kiper (ORCID: https://orcid.org/0000-0001-7244-7766)
- Rahşan Göçmen (ORCID: https://orcid.org/0000-0002-0223-9336)
- Gülen Eda Ütine (ORCID: https://orcid.org/0000-0001-6577-5542)
- Esra Işık (ORCID: https://orcid.org/0000-0003-0657-2408)
- Akçahan Akalın (ORCID: https://orcid.org/0000-0001-9770-284X)
- Tahir Atık (ORCID: https://orcid.org/0000-0002-1142-3872)
- Cansu Özşin‐Özler (ORCID: https://orcid.org/0000-0002-9366-3991)
- Dilek Yalnızoğlu (ORCID: https://orcid.org/0000-0001-9294-4305)
- Fatma Dilara Baysan (ORCID: https://orcid.org/0000-0002-1303-079X)
- Enise Avcı Durmuşalioğlu (ORCID: https://orcid.org/0000-0002-0582-8881)
- Veysel ÖZ (ORCID: https://orcid.org/0000-0002-7619-9365)
- Nursel H Elcioglu (ORCID: https://orcid.org/0000-0003-0051-6720)
- Göknur Haliloğlu (ORCID: https://orcid.org/0000-0003-1813-275X)
- Gizem Ürel Demir (ORCID: https://orcid.org/0000-0002-9928-3236)
- Meryem Uzamış Tekçiçek (ORCID: https://orcid.org/0000-0003-1179-7708)
- Kadir Işık (ORCID: https://orcid.org/0000-0001-8753-5208)
- Funda Kökali (ORCID: https://orcid.org/0000-0003-3431-2777)
Institutions
- Dicle University (TR)
- Yozgat Bozok Üniversitesi (TR)
- Eastern Mediterranean University (CY)
- Ege University (TR)
- Hacettepe University (TR)
- Marmara University (TR)
Publication Details
- Journal
- Neurology Genetics
- Published
- 2026-10-27
- DOI
- https://doi.org/10.1212/nxg.0000000000200446
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00