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. 2021 Nov-Dec;24(6):999-1001.
doi: 10.4103/aian.AIAN_1052_20. Epub 2021 Mar 27.

Von Hippel Lindau Disease Presenting as Cervical Compressive Myelopathy

Aminu Aliyar  1 , Ayush Agarwal  1 , Venugopalan Y Vishnu  1 , Anu Gupta  1 , Ajay Garg  2 , Mamta Bhushan Singh  1 , Rohit Bhatia  1 , Mv Padma Srivastava  1 , Roopa Rajan  1
Affiliations

Von Hippel Lindau Disease Presenting as Cervical Compressive Myelopathy

Aminu Aliyar et al. Ann Indian Acad Neurol. 2021 Nov-Dec.
No abstract available

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Conflict of interest statement

There are no conflicts of interest.

Figures

Figure 1
Figure 1
Sagittal (a) and axial (b) T2 -WIs show iso-hyperintense intramedullary lesion (arrows in a & c) on ventral aspect of spinal cord at C5-7 levels with multiple intradural flow-voids (arrowhead in a). The mass demonstrates homogeneous enhancement (arrows in b and d) in post-gadolinium sagittal (b) and axial (d) T1-WIs
See this image and copyright information in PMC

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References

    1. Andersen MK, Bisgaard ML, Brandt C. Surveillance in von Hippel-Lindau disease (vHL) Clin Genet. 2010;77:49–59. - PubMed
    1. Maher ER, Iselius L, Yates JR, Littler M, Benjamin C, Harris R, et al. Von Hippel-Lindau disease: A genetic study. J Med Genet. 1991;28:443–7. - PMC - PubMed
    1. Maddock IR, Moran A, Maher ER, Teare MD, Norman A, Payne SJ, et al. A genetic register for von Hippel-Lindau disease. J Med Genet. 1996;33:120–7. - PMC - PubMed
    1. Neumann HP, Wiestler OD. Clustering of features of von Hippel-Lindau syndrome: Evidence for a complex genetic locus. Lancet. 1991;337:1052–4. - PubMed
    1. Neumann HP, Berger DP, Sigmund G, Blum U, Schmidt D, Parmer RJ, et al. Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel- Lindau disease. N Engl J Med. 1993;329:1531–8. - PubMed