Suppr超能文献

支持一名患有巴德-比德尔综合征(一种罕见的复杂残疾)的聪加族学习者。

Supporting a Tsonga learner living with Bardet-Biedl syndrome, a rare complex disability.

作者信息

Shikwambana Mfungana M, Fourie Jean V

机构信息

Department of Educational Psychology, Faculty of Education, University of Johannesburg, Johannesburg, South Africa.

出版信息

Afr J Disabil. 2023 Dec 4;12:1181. doi: 10.4102/ajod.v12i0.1181. eCollection 2023.

Abstract

BACKGROUND

Bardet-Biedl syndrome (BBS) is a rare, systemic, hereditary disorder characterised by obesity, polydactyly, visual and auditory impairment, and cognitive disability. Providing quality education in appropriate schools for children who present with such complex chronic conditions is challenging.

OBJECTIVES

This study explored the dimensions of psycho-educational support needs for a child with BBS in South Africa to contribute to the improvement of early detection and holistic interventions.

METHOD

A descriptive in-depth qualitative case study of Gezani, an adolescent Tsonga boy diagnosed with BBS, was undertaken. Semi-structured interviews were conducted with his parents and teachers to ascertain the boy's psycho-educational support needs. Medical reports provided information on the complexities and prognosis of the syndrome. Observations in the classroom corroborated the learner's symptoms and behaviours.

RESULTS

Thematic content analysis revealed the key areas of support needs. Gezani's cognitive disability required a modified, slow-paced curriculum. His visual impairment required mobility orientation training and learning Braille. His emotional needs were supported with psychotherapy to maintain a sense of well-being. Medical monitoring was recommended with interventions for walking and managing his diet and weight. Speech therapy supported his communication skills.

CONCLUSION

Learners with multiple disabilities require carefully planned, individualised psycho-educational support programmes addressing their unique needs and delays with targeted remedial interventions in appropriate special needs schools.

CONTRIBUTION

This study informs educators about BBS and provides multi-faceted, holistic support. The Department of Basic Education could bring special schools and national policies in tighter alignment for learners presenting with complex disabilities.

摘要

背景

巴德-比埃尔综合征(BBS)是一种罕见的全身性遗传性疾病,其特征为肥胖、多指(趾)畸形、视力和听力障碍以及认知残疾。为患有此类复杂慢性病的儿童在合适的学校提供优质教育具有挑战性。

目的

本研究探讨了南非一名患有BBS的儿童心理教育支持需求的维度,以促进早期发现和整体干预的改善。

方法

对一名被诊断患有BBS的聪加族青少年男孩格扎尼进行了描述性深入定性案例研究。与他的父母和教师进行了半结构化访谈,以确定该男孩的心理教育支持需求。医疗报告提供了有关该综合征复杂性和预后的信息。在课堂上的观察证实了该学习者的症状和行为。

结果

主题内容分析揭示了支持需求的关键领域。格扎尼的认知残疾需要一个经过修改的、节奏较慢的课程。他的视力障碍需要行动定向训练和学习盲文。通过心理治疗来支持他的情感需求,以维持幸福感。建议进行医疗监测,并采取干预措施来帮助他行走以及管理饮食和体重。言语治疗支持他的沟通技能。

结论

患有多种残疾的学习者需要精心规划、个性化的心理教育支持计划,以满足他们的独特需求,并在合适的特殊需求学校通过有针对性的补救干预来解决他们的发育迟缓问题。

贡献

本研究让教育工作者了解了BBS,并提供了多方面的整体支持。基础教育部门可以使特殊学校和国家政策更紧密地结合起来,以满足患有复杂残疾的学习者的需求。

相似文献

1
Supporting a Tsonga learner living with Bardet-Biedl syndrome, a rare complex disability.
Afr J Disabil. 2023 Dec 4;12:1181. doi: 10.4102/ajod.v12i0.1181. eCollection 2023.
3
Evaluation of visual function and needs in adult patients with bardet-biedl syndrome.
Retina. 2014 Nov;34(11):2282-9. doi: 10.1097/IAE.0000000000000222.
4
Bardet Biedl syndrome in South Africa: A single founder mutation.
S Afr Med J. 2016 May 25;106(6 Suppl 1):S72-4. doi: 10.7196/SAMJ.2016.v106i6.11000.
6
Bardet-Biedl syndrome: a case series.
J Med Case Rep. 2022 Apr 29;16(1):169. doi: 10.1186/s13256-022-03396-6.
7
Clinical characteristics of a Japanese patient with Bardet-Biedl syndrome caused by BBS10 mutations.
Jpn J Ophthalmol. 2018 Jul;62(4):458-466. doi: 10.1007/s10384-018-0591-8. Epub 2018 Apr 17.
8
Bardet-Biedl Syndrome in an Ethiopian.
Int Med Case Rep J. 2021 Mar 19;14:177-181. doi: 10.2147/IMCRJ.S299421. eCollection 2021.
10
The importance of renal impairment in the natural history of Bardet-Biedl syndrome.
Am J Kidney Dis. 1996 Jun;27(6):776-83. doi: 10.1016/s0272-6386(96)90513-2.

引用本文的文献

1
Inclusive education pandemic: Learning barriers for children with disabilities in South Africa.
Afr J Disabil. 2024 Dec 6;13:1462. doi: 10.4102/ajod.v13i0.1462. eCollection 2024.

本文引用的文献

1
Central positional nystagmus: an update.
J Neurol. 2022 Apr;269(4):1851-1860. doi: 10.1007/s00415-021-10852-8. Epub 2021 Oct 20.
2
Bardet-Biedl syndrome: Weight patterns and genetics in a rare obesity syndrome.
Pediatr Obes. 2021 Feb;16(2):e12703. doi: 10.1111/ijpo.12703. Epub 2020 Jul 22.
4
Thoraco-Abdominal Abnormalities in Bardet-Biedl Syndrome: Situs Inversus and Heterotaxy.
J Pediatr. 2019 Jan;204:31-37. doi: 10.1016/j.jpeds.2018.08.068. Epub 2018 Oct 4.
5
6
Renal transplantation in Bardet-Biedl Syndrome.
Pediatr Nephrol. 2016 Nov;31(11):2153-61. doi: 10.1007/s00467-016-3415-4. Epub 2016 Jun 1.
7
Bardet Biedl syndrome in South Africa: A single founder mutation.
S Afr Med J. 2016 May 25;106(6 Suppl 1):S72-4. doi: 10.7196/SAMJ.2016.v106i6.11000.
8
Exploring genotype-phenotype relationships in Bardet-Biedl syndrome families.
J Med Genet. 2015 Aug;52(8):503-13. doi: 10.1136/jmedgenet-2015-103099. Epub 2015 Jun 16.
9
Bayley-III Cognitive and Language Scales in Preterm Children.
Pediatrics. 2015 May;135(5):e1258-65. doi: 10.1542/peds.2014-3039. Epub 2015 Apr 20.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验