Case report shows uncommon craniofacial abnormalities and hearing loss in a male with Hajdu-Cheney syndrome, suggesting implications for diagnosis.
Hajdu-Cheney Syndrome (HCS) is an exceedingly rare connective tissue disorder primarily manifested by skeletal abnormalities including acro-osteolysis, severe osseous demineralization, distinctive craniofacial/dental abnormalities and short stature. The syndrome is caused by gain-of-function mutations in the NOTCH2 gene, which disrupt bone remodeling and connective tissue integrity. While hearing loss is a known clinical manifestation of HCS, specific imaging findings have not been reported. We present the case of a 36-year-old male with HCS who underwent high-resolution CT of the temporal bones for evaluation of longstanding bilateral conductive hearing loss, which showed relatively symmetric, diffuse osseous demineralization of the temporal bones, with ossicular and otic capsule involvement.ABBREVIATIONS: HCS= Hajdu-Cheney Syndrome; CT = Computed Tomography; OI = Osteogenesis Imperfecta.
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Jung et al. (2025) studied this question.
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