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Anterior segment dysgenesis as a feature of Neurofibromatosis-I

Eye (2025)Cite this article

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Fig. 1: A nine-year-old girl presented with asymmetric eyes and poor vision in her left eye since early childhood.

Data availability

The data that support the findings of this study are available from the corresponding author upon reasonable request. All data needed to evaluate the conclusions in the paper is presented in the paper and/ or the Supporting Information.

References

  1. Legius E, Messiaen L, Wolkenstein P, Pancza P, Avery RA, Berman Y, et al. Revised diagnostic criteria for Neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation. Genet Med. 2021;23:1506–13.

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  2. Ly KI, Blakeley JO. The diagnosis and management of Neurofibromatosis Type 1. Med Clin North Am. 2019;103:1035–54.

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  3. Kinori M, Hodgson N, Zeid JL. Ophthalmic manifestations in Neurofibromatosis type 1. Surv Ophthalmol. 2018;63:518–33.

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Authors and Affiliations

  1. Dr Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, Delhi, India

    Manasi Tripathi, Vidit Bansal & Rajesh Sinha

Authors
  1. Manasi Tripathi
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  2. Vidit Bansal
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  3. Rajesh Sinha
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Contributions

MT: Conceptualization, patient management, manuscript writing, and editing. VB: Data retrieval, literature search. RS: Manuscript review, editing, clinician in charge.

Corresponding author

Correspondence to Manasi Tripathi.

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The authors declare no competing interests.

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The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

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Tripathi, M., Bansal, V. & Sinha, R. Anterior segment dysgenesis as a feature of Neurofibromatosis-I. Eye (2025). https://doi.org/10.1038/s41433-025-03781-7

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  • DOI: https://doi.org/10.1038/s41433-025-03781-7

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