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Morier, P., Merot, Y., Paccaud, D., Beck, D. and Frenk, E. (1990) Juvenile Chronic Granulocytic Leukemia, Juvenile Xanthogranulomas, and Neurofibromatosis. Case Report and Review of the Literature. Journal of the American Academy of Dermatology, 22, 962-965.

has been cited by the following article:

• TITLE: Neurofibromatosis Type 1 in Four Children Cases

  AUTHORS: C. Mammad, N. Mekaoui, F. Z. Ouadghiri, K. Mammad, B. S. Benjeloun Dakhama

  KEYWORDS: Neurofibromatosis Type 1, Children, Café au lait Spots, Lentiginous

  JOURNAL NAME: Neuroscience and Medicine, Vol.8 No.3, September 28, 2017

  ABSTRACT: Neurofibromatosis Type 1 (NF-1 or Von Recklinghausen disease) is an autosomal dominant genetic disease, characterized by an extreme variability of its clinical expression which is also found in the same family. Our work focuses on the exploitation of four cases of patients with NF-1 who were enrolled in the paediatric neurology consultation at Rabat Children’s Hospital. They are two infants and two children. Otherwise the diagnosis was made in front of the existence of café au lait and lentiginous spots in two boys, also the existence of café au lait spots and abnormalities in brain imaging in two girls. Thus an evolution was marked by a favorable outcome for three patients and neurological sequelae in one patient.