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 |
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| Hauptverfasser: | , , , , , , , , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
United States
John Wiley & Sons, Inc
01.11.2025
Wiley |
| Schlagworte: | |
| ISSN: | 2324-9269, 2324-9269 |
| Online-Zugang: | Volltext |
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