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Atypical Lindsay-Hemenway syndrome in a patient with Klippel-Feil syndrome: a new association? Case report and etiopathogenic review

Abstract Introduction Klippel–Feil syndrome is a rare congenital disorder characterized by the fusion of two or more cervical vertebrae. It may be associated with malformations in other systems, including auditory abnormalities. Approximately 30% of patients present with hearing loss; however, the f...

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Bibliografiset tiedot
Päätekijät: Vicente Martín Moreno, Beatriz Alonso Serna, Amanda Martín Fernández, Elizabeth Rosario Coaquira Condori, Natalia Sánchez Prida
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Springer 2026-04-01
Sarja:Journal of Rare Diseases
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Linkit:https://doi.org/10.1007/s44162-026-00194-2
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