Dental abnormalities observed in the oculo-facio-cardio-dental (OFCD) syndrome present in two Czech families bearing novel de novo BCOR pathogenic variants
Language English Country England, Great Britain Media electronic
Document type Journal Article, Case Reports
Grant support
ZD-ZDOVA2-001
European Accounting Association
24-10324S
Grantová Agentura České Republiky
NW24-06-00083
Agentura Pro Zdravotnický Výzkum České Republiky
PubMed
39438869
PubMed Central
PMC11494979
DOI
10.1186/s12903-024-05005-y
PII: 10.1186/s12903-024-05005-y
Knihovny.cz E-resources
- Keywords
- BCOR, Congenital cataract, Dental anomalies, Novel pathogenic variants, OFCD syndrome, Syndromic microphthalmia-2 radiculomegaly,
- MeSH
- Eye Abnormalities genetics MeSH
- Tooth Abnormalities * genetics MeSH
- Heart Septal Defects MeSH
- Child MeSH
- Adult MeSH
- Phenotype MeSH
- Genetic Diseases, X-Linked MeSH
- Cataract genetics congenital MeSH
- Humans MeSH
- Microphthalmos * genetics MeSH
- Adolescent MeSH
- Abnormalities, Multiple genetics MeSH
- Proto-Oncogene Proteins * genetics MeSH
- Radiography, Panoramic MeSH
- Repressor Proteins * genetics MeSH
- Pedigree MeSH
- Heart Defects, Congenital genetics complications MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Humans MeSH
- Adolescent MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Geographicals
- Czech Republic MeSH
- Names of Substances
- BCOR protein, human MeSH Browser
- Proto-Oncogene Proteins * MeSH
- Repressor Proteins * MeSH
BACKGROUND: The oculo-facio-cardio-dental syndrome (OFCD) is an ultra-rare multiple congenital anomaly. This report describes clinical findings emphasising dental phenotype in five, molecularly confirmed, female cases from two Czech families. CASE PRESENTATION: Dental examinations were carried out. An orthopantomogram was taken in three patients, and all patients' intraoral cavities and teeth were photographed. Exome sequencing was performed in both probands. Results were validated by Sanger DNA sequencing which was also used to follow segregation of the variants in first-degree relatives. Dental abnormalities and congenital cataracts were present in all five cases, whilst other signs were variable and included facial dysmorphism, microphthalmia, and cardiac and skeletal abnormalities. Two individuals had cleft lip and/or cleft palate. Radiculomegaly occurred in three patients with permanent teeth and was diagnosed on orthopantomograms. Two patients had agenesis of permanent teeth. Malocclusion was also present in two patients due to crowding and a Class III malocclusion and mandibular overjet. De novo novel pathogenic variants in the BCOR gene were identified; c.2382del p.(Lys795Argfs*12) and c.3914dup p.(Gln1306Alafs*20) and co-segregated with the disease in each family. CONCLUSIONS: The OFCD syndrome has a unique dental phenotype and dentists should be aware of signs of this ultra-rare genetic disorder. All patients with congenital cataracts and dental abnormalities, including those without a family history, should be referred for genetic testing and indicated to specialised dental care.
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