Identifying the unmet needs of patients with neurofibromatosis type 1 in Singapore

Agnes Lim, Zi Yang Chua, Celestine Loh, Priyadharshini Suresh, Jeanette Yuen, Manasadevi Kartikeyan, Zhang Zewen, Jianbang Chiang, Mark Jean Aan Koh, Nikki Wen Yan Fong, Ee Shien Tan, Joanne Ngeow*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with tumour predisposition, and patients often face neuropsychiatric and psychosocial challenges. This study aimed to identify unmet needs of NF1 patients in Singapore to enhance patient care and service delivery. Methods: 20 patients who were clinically or genetically diagnosed with NF1 were recruited for in-depth interviews. Interviews were transcribed verbatim and analysed using thematic analysis. Results: Five themes emerged from thematic analysis: (1) NF1 trajectory begins from childhood; (2) Coming to terms with body and self; (3) Perceived acceptance drives disclosure patterns; (4) Need for specialised NF1 care; (5) Building local awareness and connections. Six key unmet needs were identified, namely the need for: (1) Optimised multidisciplinary NF1 care; (2) Management of neurological symptoms; (3) Management of cutaneous lesions; (4) Financial coverage for NF1; (5) Early NF1 screening; (6) Local awareness and support groups. Conclusion: Addressing these needs can lead to actionable steps for improving care and quality of life for NF1 patients in Singapore.

Original languageEnglish
Article numberjmg-2025-110702
JournalJournal of Medical Genetics
DOIs
Publication statusAccepted/In press - 2025
Externally publishedYes

Bibliographical note

Publisher Copyright:
© Author(s) (or their employer(s)) 2025.

ASJC Scopus Subject Areas

  • Genetics
  • Genetics(clinical)

Keywords

  • Genetic Counseling
  • Health Services Research
  • Oncology
  • Patient Care
  • Quality of Health Care

Fingerprint

Dive into the research topics of 'Identifying the unmet needs of patients with neurofibromatosis type 1 in Singapore'. Together they form a unique fingerprint.

Cite this