Living With Hypochondroplasia: A Qualitative Exploration of Children's and Caregivers' Experiences, Challenges, and Unmet Needs

Hypochondroplasia (HCH) is a rare genetic skeletal dysplasia characterized by short stature, disproportionate limbs, and complications such as learning differences. Currently, no treatments are approved to address HCH-related short stature, which can adversely affect quality of life. This study aime...

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Veröffentlicht in:Molecular genetics & genomic medicine Jg. 13; H. 11; S. e70151 - n/a
Hauptverfasser: Oehrlein, Elisabeth M., Pekala, Reni, Cavallaro, Stacie, Cho, Margaret, Crews, Chandler, Dauber, Andrew, Saxena, Ankita, Vandigo, Joe, Reese, Emily S.
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States John Wiley & Sons, Inc 01.11.2025
Wiley
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ISSN:2324-9269, 2324-9269
Online-Zugang:Volltext
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