Expanding the clinical spectrum: A case report of the first Jordanian presentation of KID syndrome with neurological and skeletal anomalies beyond the classical triad
This case highlights potential atypical manifestations of KID syndrome, including seizures, ventriculomegaly, torticollis, and hip dysplasia, that may reflect a broader but under-recognized phenotypic range.
Authors
- Malek Abu Rumman
- Safaa Al-Tawalbeh
- Anas Satari (ORCID: https://orcid.org/0009-0000-2251-6911)
- M. Maaita (ORCID: https://orcid.org/0009-0000-6994-3400)
- Mohannad Thafer Yamin
- Osama Aloudat
- Yara Abukhaled (ORCID: https://orcid.org/0009-0007-9088-0759)
- Rama Al-Bustanji
- Mu‘nis Muneeb Mohammad Alrashdan
- Aya Khaled D. Salah
- Gharam Ghalyon
- Nizar Al-Rabadi
- Hamzeh K. Bany Younis
- Bayan K. AlRababah
Institutions
- University of Jordan (JO)
- Jordan University of Science and Technology (JO)
- University of Tennessee Health Science Center (US)
- Mutah University (JO)
- King Hussein Cancer Center (JO)
- Jordan Hospital (JO)
- King Hussein Medical Center (JO)
- Al al-Bayt University (JO)
- Cardinal Glennon Children’s Medical Center (US)
- The Farah Hospital (JO)
Publication Details
- Journal
- Medicine
- Published
- 2025-11-21
- DOI
- https://doi.org/10.1097/md.0000000000045577
- Citations
- 1
- Primary Topic
- Genetic Syndromes and Imprinting
- Type
- article
- Field-Weighted Citation Impact
- 1.82