Exploring the health, education and social support needs of individuals diagnosed with SATB2 Associated Syndrome and their families living in Australia

Rare Pub Date : 2025-01-01 DOI:10.1016/j.rare.2025.100094
Maryanne Abouharb , Dalal Dawood Baumgartner , Sarah Wilkes-Gillan , Dave Parsons , Lauren Parsons , Iva Strnadová , Elizabeth Emma Palmer , Ryan Chen , Natalie Munro
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Abstract

Background

SATB2 Associated Syndrome is a rare genetic neurodevelopmental condition affecting multiple developmental areas including cognition, speech, behaviour and dentition. Currently, a lack of lived experience research exists involving Australian families and individuals diagnosed with SATB2 Associated Syndrome.

Aim

The study aimed to enhance understanding of support needs and challenges and access to and experience with health, education, family and community-based support services for individuals diagnosed with SATB2 Associated Syndrome and their families.

Method

The study utilised a co-design approach with SATB2 Connect, a not-for-profit organisation supporting Australian families and individuals diagnosed with SATB2 Associated Syndrome. An exploratory cross-sectional online survey employed purposive sampling, targeting individuals diagnosed with SATB2 Associated Syndrome and their families. The analysis encompassed descriptive statistics and content analysis.

Result

Out of 32 eligible/invited families, 14 responded representing rural and metropolitan areas across five states/territories. Respondents described challenges faced by individuals diagnosed with SATB2 Associated Syndrome, including communication (100 %), reasoning (100 %), dental care (93 %) and behaviour (86 %). Barriers included limited access to information, therapy and education services. Key therapy obstacles encompassed availability (64 %), multidisciplinary services (57 %) and cost (43 %). Educational barriers included lack of multidisciplinary services (60 %) and educators’ unfamiliarity (40 %) with SATB2 Associated Syndrome. Qualitative analysis supplemented quantitative results, revealing diverse experiences and social support needs.

Conclusion

In this first Australian study exploring the health, education and social support needs of individuals diagnosed with SATB2 Associated Syndrome and their families, participants reported accessing health, therapy, education and social supports. Unmet needs were reported related to receiving information about therapy and finding specialist practitioners and support workers with more assistance needed in overcoming therapy and education barriers as well as social support. These findings will drive advocacy, raise syndrome awareness and guide research priorities, potentially enhancing intervention, health and education support services.
探讨在澳大利亚生活的被诊断为SATB2相关综合征的个人及其家人的健康、教育和社会支持需求
satb2相关综合征是一种罕见的遗传性神经发育疾病,影响认知、言语、行为和牙齿等多个发育领域。目前,缺乏涉及澳大利亚被诊断为SATB2相关综合征的家庭和个人的生活经验研究。目的本研究旨在增进对支助需求和挑战的了解,以及为被诊断为SATB2相关综合征的个人及其家庭提供保健、教育、家庭和社区支助服务的机会和经验。方法:本研究采用了与SATB2 Connect(一个支持被诊断为SATB2相关综合征的澳大利亚家庭和个人的非营利组织)共同设计的方法。一项探索性的横断面在线调查采用有目的的抽样,针对被诊断为SATB2相关综合征的个体及其家庭。分析包括描述性统计和内容分析。结果在32个合格/受邀的家庭中,有14个回应了来自5个州/地区的农村和大都市地区。受访者描述了被诊断为SATB2相关综合征的个体所面临的挑战,包括沟通(100 %)、推理(100 %)、牙科保健(93 %)和行为(86 %)。障碍包括获得信息、治疗和教育服务的机会有限。主要的治疗障碍包括可获得性(64% %)、多学科服务(57% %)和费用(43% %)。教育障碍包括缺乏多学科服务(60% %)和教育工作者不熟悉SATB2相关综合征(40% %)。定性分析补充了定量结果,揭示了不同的经历和社会支持需求。在澳大利亚的第一项研究中,研究人员探索了被诊断为SATB2相关综合征的个体及其家庭的健康、教育和社会支持需求,参与者报告了获得健康、治疗、教育和社会支持的情况。据报告,未满足的需求涉及接收有关治疗的信息和寻找在克服治疗和教育障碍以及社会支持方面需要更多援助的专业从业人员和支助工作者。这些发现将推动宣传,提高对综合症的认识,并指导研究重点,从而可能加强干预、卫生和教育支持服务。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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