Coping and quality of life of parents of children with achondroplasia—a narrative review

• Adekunle Adedeji,
• Adekunle Adedeji,
• Stefanie Witt,
• Stefanie Witt,
• Florian Innig,
• Inês Alves,
• Chiara Provasi,
• Marco Sessa,
• Klaus Mohnike,
• Klaus Mohnike,
• Julia Quitmann,
• Julia Quitmann

Affiliations

Adekunle Adedeji

Department of Social Work, Hamburg University of Applied Sciences, Hamburg, Germany

Adekunle Adedeji

Department of Medical Psychology, University Medical Center, Hamburg-Eppendorf, Hamburg, Germany

Stefanie Witt

Department of Social Work, Hamburg University of Applied Sciences, Hamburg, Germany

Stefanie Witt

Department of Medical Psychology, University Medical Center, Hamburg-Eppendorf, Hamburg, Germany

Florian Innig

Federal Association for People of Short Stature and their Families (Bundesverband Kleinwüchsige Menschen und ihre Familien e.V.), BKMF, Bremen, Germany

Inês Alves

National Patient Organization for Skeletal Dysplasias – ANDO, School of Health and Human Development, University of Évora - CHRC, Évora, Portugal

Chiara Provasi

Italian Association on Achondroplasia (Associazione per l’Informazione e lo studio dell’acondroplasia) AISAC, Milan, Italy

Marco Sessa

Italian Association on Achondroplasia (Associazione per l’Informazione e lo studio dell’acondroplasia) AISAC, Milan, Italy

Klaus Mohnike

Federal Association for People of Short Stature and their Families (Bundesverband Kleinwüchsige Menschen und ihre Familien e.V.), BKMF, Bremen, Germany

Klaus Mohnike

Children’s Hospital, Otto-von-Guericke-University, Magdeburg, Germany

Julia Quitmann

Department of Social Work, Hamburg University of Applied Sciences, Hamburg, Germany

Julia Quitmann

Department of Medical Psychology, University Medical Center, Hamburg-Eppendorf, Hamburg, Germany