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    The Rare Association of Congenital Glaucoma, Giant Melanocytic Nevus, Alopecia, and Hypospadias in an Egyptian Child With Neurofibromatosis Type 1: A Case Report

    Abdelrahim A. Sadek, Mohammed A. Aladawy, Tarek Mansour … Elsayed Abdelkreem
    Studysummary This case report adds to the understanding of neurofibromatosis type 1 by documenting an Egyptian child with the condition alongside multiple unusual congenital anomalies, highlighting the importance of considering NF1 when these features are present.
    Automatically generated from the study's abstract, not written by a person, and not a review of the full paper. Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer
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    Research cited in this study 1

    1. Comparison of Hair Manifestations in Cardio-Facio-Cutaneous and Costello Syndromes Highlights the Influence of the RAS Pathway on Hair Growth Journal of the European Academy of Dermatology and Venereology · 2019