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. 2023 Jul-Aug;89(4):643.
doi: 10.25259/IJDVL_1144_2021.

A rare case of aggressive phenotype (Wishart) of neurofibromatosis type 2

Pankaj Das  1 , Gautam Kumar Singh  1 , G B Prashantha  1 , Sanghita Barui  2 , Debashish Saumya Ranjan Das  3 , Saurabh Kushwaha  4 , Lav Pathak  5 , Akanksha Gupta  1
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Free article

A rare case of aggressive phenotype (Wishart) of neurofibromatosis type 2

Pankaj Das et al. Indian J Dermatol Venereol Leprol. 2023 Jul-Aug.
Free article
No abstract available

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References

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    1. Firestone BK,Arias JD,Shields CL,Shields JA,. Bilateral combined hamartomas of the retina and retinal pigment epithelium as the presenting feature of neurofibromatosis type 2 (Wishart Type). J Pediatr Ophthalmol Strabismus. 2014; 51:93-710
    1. Brosius S,. A history of von Recklinghausen’s NF1. J Hist Neurosci. 2010; 19:333-48
    1. Ruggieri M,Praticò AD,Caltabiano R,Polizzi A,. Early history of the different forms of neurofibromatosis from ancient Egypt to the British Empire and beyond: First descriptions, medical curiosities, misconceptions, landmarks, and the persons behind the syndromes. Am J Med Genet A. 2018; 176:515-50
    1. Ardern-Holmes S,Fisher G,North K,. Neurofibromatosis type 2. J Child Neurol. 2017; 32:9-22

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