AI Article Synopsis
- Osteogenesis imperfecta (OI) is a genetic bone disorder leading to frequent fractures, with most cases linked to specific gene mutations, predominantly inherited in an autosomal dominant manner.
- Recent studies have found a wider range of genes associated with sporadic and familial cases of OI, particularly among offspring of unaffected or consanguineous parents.
- The research highlights the importance of thorough genetic analysis, revealing not only common mutations but also rare variants linked to other conditions, aiding in the clinical diagnosis and understanding of OI's genetic complexity.
Article Abstract
Background: Osteogenesis imperfecta (OI) is a heterogeneous bone disorder characterized by recurrent fractures. Although most cases of OI have heterozygous mutations in or and show autosomal dominant inheritance, during the last years there has been an explosion in the number of genes responsible for both recessive and dominant forms of this condition. Herein, we have analyzed a cohort of patients with OI, all offspring of unaffected parents, to determine the spectrum of variants accounting for these cases. Twenty patients had nonrelated parents and were sporadic, and 21 were born to consanguineous relationships.
Methods: Mutation analysis was performed using a next-generation sequencing gene panel, homozygosity mapping, and whole exome sequencing (WES).
Results: Patients offspring of nonconsanguineous parents were mostly identified with or heterozygous changes, although there were also a few cases with and heterozygous mutations. Only one sporadic patient was a compound heterozygote for two recessive mutations. Patients offspring of consanguineous parents showed homozygous changes in a variety of genes including ,,,,,,, and . In addition, two patients born to consanguineous parents were found to have de novo heterozygous mutations demonstrating that causative variants in the collagen I structural genes cannot be overlooked in affected children from consanguineous couples. Further to this, WES analysis in probands lacking mutations in OI genes revealed deleterious variants in ,, and , which are associated with congenital indifference to pain (CIP) and Fanconi-Bickel syndrome (FBS).
Conclusion: This work provides useful information for clinical and genetic diagnosis of OI patients with no positive family history of this disease. Our data also indicate that CIP and FBS are conditions to be considered in the differential diagnosis of OI and suggest a positive role of and in bone development.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241205 | PMC |
| http://dx.doi.org/10.1002/mgg3.257 | DOI Listing |
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