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Triad of Microcephaly, Pedal Lymphedema, and Pigmentary Eye Changes: A Visual Diagnosis

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References

  1. Ostergaard P, Simpson MA, Mendola A, et al. Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy. Am J Hum Genet. 2012;90:356–62.

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Author notes

  1. Pooja Jindal and Pradeep Kumar Gunasekaran contributed equally and share joint first authorship.

Authors and Affiliations

  1. Department of Pediatrics, All India Institute of Medical Sciences, Jodhpur-342005, Rajasthan, India

    Pooja Jindal, Pradeep Kumar Gunasekaran, Sujatha Manjunathan, Kuldeep Singh & Lokesh Saini

  2. Department of Ophthalmology, All India Institute of Medical Sciences, Jodhpur-342005, Rajasthan, India

    Jyoti Shakrawal Varshney

Authors
  1. Pooja Jindal
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  2. Pradeep Kumar Gunasekaran
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  3. Sujatha Manjunathan
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  4. Jyoti Shakrawal Varshney
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  5. Kuldeep Singh
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  6. Lokesh Saini
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Correspondence to Lokesh Saini.

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Jindal, P., Gunasekaran, P.K., Manjunathan, S. et al. Triad of Microcephaly, Pedal Lymphedema, and Pigmentary Eye Changes: A Visual Diagnosis. Indian J Pediatr 91, 195–196 (2024). https://doi.org/10.1007/s12098-023-04568-y

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  • DOI: https://doi.org/10.1007/s12098-023-04568-y

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