The Rare Association of Congenital Glaucoma, Giant Melanocytic Nevus, Alopecia, and Hypospadias in an Egyptian Child With Neurofibromatosis Type 1: A Case Report
September 2024
in “
Egyptian Journal of Medical Human Genetics
”
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.
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