Temporal Bone CT Findings in Hajdu-Cheney Syndrome: Case Report with Review of the Literature

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.

Authors

Institutions

Publication Details

Journal
American Journal of Neuroradiology
Published
2025-12-01
DOI
https://doi.org/10.3174/ajnr.a9121
Primary Topic
Craniofacial Disorders and Treatments
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Temporal Bone CT Findings in Hajdu-Cheney Syndrome: Case Report with Review of the Literature

Daniel J. Kim, Ryan A. Bartholomew, Hugh D. Curtin, Hillary R. Kelly et al.
American Journal of Neuroradiology
Craniofacial Disorders and Treatments
article

Temporal Bone CT Findings in Hajdu-Cheney Syndrome: Case Report with Review of the Literature

Daniel J. Kim, Ryan A. Bartholomew, Hugh D. Curtin, Hillary R. Kelly, David H. Jung, Manuel Patiño
article en

Abstract

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.

American Journal of Neuroradiology
Massachusetts Eye and Ear Infirmary (US), Beth Israel Deaconess Medical Center (US)
Openalex Percentile: Top 61%
Craniofacial Disorders and Treatments
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.