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.

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Journal
Neurology Genetics
Published
2026-10-27
DOI
https://doi.org/10.1212/nxg.0000000000200446
Primary Topic
Genomics and Rare Diseases
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article
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article

Comprehensive Clinical, Neuroradiologic, and Oral Health of 23 Individuals With MOPDII

İsmet Rezani Toptancı, Nagihan Koç, Pelin Özlem Şimşek‐Kiper, Rahşan Göçmen et al.
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Neurology Genetics
Genomics and Rare Diseases
article

Comprehensive Clinical, Neuroradiologic, and Oral Health of 23 Individuals With MOPDII

İsmet Rezani Toptancı, Nagihan Koç, Pelin Özlem Şimşek‐Kiper, Rahşan Göçmen, Gülen Eda Ütine, Esra Işık, Akçahan Akalın, Tahir Atık, Cansu Özşin‐Özler, Dilek Yalnızoğlu, Fatma Dilara Baysan, Enise Avcı Durmuşalioğlu, Veysel ÖZ, Nursel H Elcioglu, Göknur Haliloğlu, Gizem Ürel Demir, Meryem Uzamış Tekçiçek, Kadir Işık, Funda Kökali
article en

Abstract

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.

Neurology GeneticsVol. 12(6)
Dicle University (TR), Yozgat Bozok Üniversitesi (TR), Eastern Mediterranean University (CY), Ege University (TR), Hacettepe University (TR), Marmara University (TR)
Good health and well-being
Openalex Percentile: Top 14%
Genomics and Rare Diseases
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