Neurofibromatosis type 1 and pregnancy outcome: A case report

Vlora Ademi Ibishi, Hajrullah Latifi, Lena Ibishi, Anne Malin

Background: Neurofibromatosis is a genetic disorder with high variability of clinical expression. Cutaneous manifestations such as café-au-lait spots, freckling patterns, and dermal neurofibromas, are the most distinguishable and common signs appearing in the vast majority of individuals with NF-1. Instances where  a patient is both pregnant …

Posted in 2023 Volume 22 – Issue 2 Tagged , ,

Neurofibromatosis-1 and Pregnancy: Case report

Kalmantis K, Petsa A, Daskalakis G, Alexopoulos E, Korovesi E, Antsaklis P, Karagkiouzis T

Introduction: Neurofibromatosis type-1 (NF-1) is one of the most common genetic diseases following an autosomal dominant inheritance pattern. Maternal and fetal complications have been reported. Purpose: To present a very interesting and rare case report regarding neurofibromatosis – 1 (NF-1) in pregnancy and to create a complete review concerning this genetic disease …

Posted in 2018 Volume 17 – Issue 2 Tagged , ,