Case report: a delayed diagnosis of Turner’s syndrome in aboriginal adolescence in primary care
Turner syndrome is a genetic disorder characterized by a partial or complete loss of one X chromosome in females. This case report describes a 16-year-old Aboriginal adolescent who presented with amenorrhea and developmental challenges in primary care on a community visit. The patient's medical...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
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Universiti Putra Malaysia Press
2024
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| Online Access: | http://psasir.upm.edu.my/id/eprint/119340/ http://psasir.upm.edu.my/id/eprint/119340/1/119340.pdf |
| _version_ | 1848867939292282880 |
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| author | Thew, Hui Zhu Fong, Yan Bin Fong, Wen Yuan Loo, Cheng Yee Choy, Ja Shen Ng, Chee Han |
| author_facet | Thew, Hui Zhu Fong, Yan Bin Fong, Wen Yuan Loo, Cheng Yee Choy, Ja Shen Ng, Chee Han |
| author_sort | Thew, Hui Zhu |
| building | UPM Institutional Repository |
| collection | Online Access |
| description | Turner syndrome is a genetic disorder characterized by a partial or complete loss of one X chromosome in females. This case report describes a 16-year-old Aboriginal adolescent who presented with amenorrhea and developmental challenges in primary care on a community visit. The patient's medical history revealed a delay in speech development, poor academic performance, and limited literacy skills. Physical examination demonstrated characteristic Turner Syndrome features such as slanted eyes, a flat nasal bridge, a webbed neck, cubitus valgus, short metatarsals, and atrophic genitalia. Karyotyping confirmed the diagnosis of Turner Syndrome (45, X). In addition, the patient exhibited growth retardation, with height and weight measurements below the 3rd centile. Management included a referral to obstetrics and gynaecology for growth hormone therapy, aortic aneurysm and bone marrow density monitoring, and genetic counselling for the family. This case emphasizes the importance of early diagnosis, the challenges in diagnosing TS in rural areas and multidisciplinary care for patients with Turner Syndrome to address the condition's medical and developmental aspects. |
| first_indexed | 2025-11-15T14:44:28Z |
| format | Article |
| id | upm-119340 |
| institution | Universiti Putra Malaysia |
| institution_category | Local University |
| language | English |
| last_indexed | 2025-11-15T14:44:28Z |
| publishDate | 2024 |
| publisher | Universiti Putra Malaysia Press |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | upm-1193402025-08-15T01:52:03Z http://psasir.upm.edu.my/id/eprint/119340/ Case report: a delayed diagnosis of Turner’s syndrome in aboriginal adolescence in primary care Thew, Hui Zhu Fong, Yan Bin Fong, Wen Yuan Loo, Cheng Yee Choy, Ja Shen Ng, Chee Han Turner syndrome is a genetic disorder characterized by a partial or complete loss of one X chromosome in females. This case report describes a 16-year-old Aboriginal adolescent who presented with amenorrhea and developmental challenges in primary care on a community visit. The patient's medical history revealed a delay in speech development, poor academic performance, and limited literacy skills. Physical examination demonstrated characteristic Turner Syndrome features such as slanted eyes, a flat nasal bridge, a webbed neck, cubitus valgus, short metatarsals, and atrophic genitalia. Karyotyping confirmed the diagnosis of Turner Syndrome (45, X). In addition, the patient exhibited growth retardation, with height and weight measurements below the 3rd centile. Management included a referral to obstetrics and gynaecology for growth hormone therapy, aortic aneurysm and bone marrow density monitoring, and genetic counselling for the family. This case emphasizes the importance of early diagnosis, the challenges in diagnosing TS in rural areas and multidisciplinary care for patients with Turner Syndrome to address the condition's medical and developmental aspects. Universiti Putra Malaysia Press 2024 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/119340/1/119340.pdf Thew, Hui Zhu and Fong, Yan Bin and Fong, Wen Yuan and Loo, Cheng Yee and Choy, Ja Shen and Ng, Chee Han (2024) Case report: a delayed diagnosis of Turner’s syndrome in aboriginal adolescence in primary care. Malaysian Journal of Medicine and Health Sciences, 20 (5). art. no. undefined. pp. 430-433. ISSN 1675-8544; eISSN: 2636-9346 https://medic.upm.edu.my/upload/dokumen/2024093017032551_MJMHS_1177.pdf 10.47836/mjmhs20.5.52 |
| spellingShingle | Thew, Hui Zhu Fong, Yan Bin Fong, Wen Yuan Loo, Cheng Yee Choy, Ja Shen Ng, Chee Han Case report: a delayed diagnosis of Turner’s syndrome in aboriginal adolescence in primary care |
| title | Case report: a delayed diagnosis of Turner’s syndrome in aboriginal adolescence in primary care |
| title_full | Case report: a delayed diagnosis of Turner’s syndrome in aboriginal adolescence in primary care |
| title_fullStr | Case report: a delayed diagnosis of Turner’s syndrome in aboriginal adolescence in primary care |
| title_full_unstemmed | Case report: a delayed diagnosis of Turner’s syndrome in aboriginal adolescence in primary care |
| title_short | Case report: a delayed diagnosis of Turner’s syndrome in aboriginal adolescence in primary care |
| title_sort | case report: a delayed diagnosis of turner’s syndrome in aboriginal adolescence in primary care |
| url | http://psasir.upm.edu.my/id/eprint/119340/ http://psasir.upm.edu.my/id/eprint/119340/ http://psasir.upm.edu.my/id/eprint/119340/ http://psasir.upm.edu.my/id/eprint/119340/1/119340.pdf |