TL;DR
A 13-year-old female with a known diagnosis of Apert syndrome who presented with progressively worsening dental pain over one month, associated with temporal headaches and difficulty chewing is described.
Neurofibromatosis type 1 (NF1) is a neurocutaneous disorder with an incidence of 1 in 3000 live births, and facial bone involvement is. Submucosal cleft palate is a rare association with this condition. This report presents monozygotic 13-year-old twins with suspected NF1 who were referred from the orthodontic departme...
Williams–Beuren syndrome (WBS) is a rare multisystem genetic disorder caused by microdeletion at chromosome 7q11.23. This case report describes the orofacial manifestations and management of a 11year old male child with WBS. The medical history revealed global developmental delay, mild intellectual disability, impaired...
Robinow syndrome is a rare genetically heterogeneous skeletal dysplasia characterized by mesomelic limb shortening, vertebral segmentation defects, brachydactyly, and distinctive craniofacial features. Although several oral and dental manifestations have been reported, developmental dental anomalies such as concrescenc...
Background Crouzon′s syndrome is a rare autosomal dominant craniosynostosis disorder characterized by midfacial hypoplasia due to premature fusion of the coronal and sagittal sutures. Facial features are typical in the form of a hypoplastic maxilla, shallow orbits, and mandibular prognathism. The condition is usually d...
Charcot–Marie–Tooth (CMT) disease is an inherited motor and sensory neuropathy that typically presents with cavovarus foot deformity. Pes planovalgus is uncommon in CMT and, while noted incidentally in multicenter cohort studies of CMT4B subtypes, has not been described as the predominant orthopedic manifestation in a...
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