https://mirt.tsnmjournals.org/articles/lesssupgreater99lesssupgreatermtc-mdp-bone-scintigraphy-in-a-case-of-x-linked-spondyloepiphyseal-dysplasia-tarda/doi/mirt.galenos.2025.83713

Spondyloepiphyseal dysplasia tarda (SEDT) is a rare X-linked skeletal disorder affecting the spine and long bones, leading to short stature, spinal deformities, and joint stiffness. It is caused by genetic mutations, and primarily affects males. Diagnosis is confirmed by imaging and genetic testing. We report the case of a 33 years old patient with a history of X-linked SEDT, who presented with pain in the lower limbs and pelvis, accompanied by limited mobility. Bone scan with <sup>99</sup>mTc-methylene diphosphonate (MDP) revealed a polyostotic SEDT involvement, periarticular ossifications, and bony bridges in the active phase. The authors highlight the role of bone scan with <sup>99</sup>mTc-MDP in diagnosing this rare disease.

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Publication Details

Journal
Molecular Imaging and Radionuclide Therapy
Published
2025-11-26
DOI
https://doi.org/10.4274/mirt.galenos.2025.83713
Primary Topic
Connective tissue disorders research
Type
article
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article

https://mirt.tsnmjournals.org/articles/lesssupgreater99lesssupgreatermtc-mdp-bone-scintigraphy-in-a-case-of-x-linked-spondyloepiphyseal-dysplasia-tarda/doi/mirt.galenos.2025.83713

Salah Nabih Oueriagli, Omar Ait Sahel, Abderrahim Doudouh, Yassir Benameur et al.
Molecular Imaging and Radionuclide Therapy
Connective tissue disorders research
article

https://mirt.tsnmjournals.org/articles/lesssupgreater99lesssupgreatermtc-mdp-bone-scintigraphy-in-a-case-of-x-linked-spondyloepiphyseal-dysplasia-tarda/doi/mirt.galenos.2025.83713

Salah Nabih Oueriagli, Omar Ait Sahel, Abderrahim Doudouh, Yassir Benameur, Meryem Aboussabr, Ikram Zahfir
article en

Abstract

Spondyloepiphyseal dysplasia tarda (SEDT) is a rare X-linked skeletal disorder affecting the spine and long bones, leading to short stature, spinal deformities, and joint stiffness. It is caused by genetic mutations, and primarily affects males. Diagnosis is confirmed by imaging and genetic testing. We report the case of a 33 years old patient with a history of X-linked SEDT, who presented with pain in the lower limbs and pelvis, accompanied by limited mobility. Bone scan with <sup>99</sup>mTc-methylene diphosphonate (MDP) revealed a polyostotic SEDT involvement, periarticular ossifications, and bony bridges in the active phase. The authors highlight the role of bone scan with <sup>99</sup>mTc-MDP in diagnosing this rare disease.

Molecular Imaging and Radionuclide TherapyVol. 35(1)
Mohammed V University (MA)
Openalex Percentile: Top 61%
Connective tissue disorders research
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