Transition services in 22q11 deletion syndrome: Hit or miss.

ABSTRACT:

Introduction

22q11 deletion syndrome (22q11DS) is a rare genetic condition and the most common microdeletion in humans. The symptomatology is broad and variable between individuals. It is usually diagnosed in childhood and requires a multidisciplinary lifelong approach including a structured transitional care process. This study therefore seeks to enrich our understanding of transitional care for individuals with 22q11DS by exploring the insights from healthcare professionals (HCPs) from Europe and Canada with multidisciplinary backgrounds.

Methods

This interview study was part of a larger mixed-methods research project, with the qualitative component concentrating on gathering insights from HCPs involved in patient care through semi-structured interviews. We conducted quali

SUBMITTER: Ayoub S 

PROVIDER: S-EPMC12481110 | biostudies-literature | 2025

REPOSITORIES: biostudies-literature