Iris Localization of Neurofibromatosis Type 1: About 3 Cases

Authors

  • Lucrèce Joanelle Vydalie ERIGA Department of Ophthalmology, Military Hospital of Instruction Mohamed V, Rabat, Morocco
  • Filali Zineb Ophthalmology department A, specialty hospital of Rabat, Morocco
  • Ricardo MENDES Department of Ophthalmology, Military Hospital of Instruction Mohamed V, Rabat, Morocco
  • Arnaud Hugues Yempabou YONLI Department of Ophthalmology, Military Hospital of Instruction Mohamed V, Rabat, Morocco
  • Yassine Mouzari Department of Ophthalmology, Military Hospital of Instruction Mohamed V, Rabat, Morocco
  • Abdelbarre Oubaaz Department of Ophthalmology, Military Hospital of Instruction Mohamed V, Rabat, Morocco

DOI:

https://doi.org/10.55677/IJCSMR/V4I5-01/2024

Keywords:

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Abstract

Von Recklinghausen's disease or neurofibromatosis type I (NF1) is the most common phacomatosis [1].

It is a relatively common genetic disease. The ophthalmological manifestations of type I neurofibromatosis are many and varied.

References

Wolkenstein P, Zeller J et Ismaili N Neurofibromatoses Elsevier Paris 2002 ; 98-755-A-10

Gontier MF, Piussanch, Ribourg B, Petit J, Regnet C, Boudailliez B Histopathogénie des phacomatoses La Médecine Infantile, 1977 ;1 :231-245.

Dolfus H, Richard S, Flament J Phacomatoses et oeil Ency Med Chir 2000; 21-470-D-20.

Daoudi C, Daoudi R. Nodules de Lisch dans la maladie de Von Recklinghausen [Lisch nodules in Von Recklinghausen disease]. Pan Afr Med J. 2014 Oct 20;19:173.

L. Menard, G. Magnaval, A. Donnio, L. Ayeboua, R. Richer, H. Merle, Les nodules de Lisch : description de deux cas cliniques et signification, Volume 1077, Issue 9, 11/2001, Pages 912-1013, ISSN 0181-5512.

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Published

2024-05-01

How to Cite

Lucrèce Joanelle Vydalie ERIGA, Filali Zineb, Ricardo MENDES, Arnaud Hugues Yempabou YONLI, Yassine Mouzari, & Abdelbarre Oubaaz. (2024). Iris Localization of Neurofibromatosis Type 1: About 3 Cases. International Journal of Clinical Science and Medical Research, 4(5), 145–148. https://doi.org/10.55677/IJCSMR/V4I5-01/2024