A rare case of spinal plexiform neurofibromas in a 9 year old Indian child with Neurofibromatosis Noonan syndrome Clinical and neuroradiological insights

Neurofibromatosis Noonan Syndrome (NFNS) is a rare RASopathy resulting from a variant NF1 gene mutation, characterized by a combination of features from both Neurofibromatosis type 1 (NF1) and Noonan Syndrome (NS).

Authors

Publication Details

Journal
Annals of Pediatrics and Neonatal Care
Published
2025-03-21
DOI
https://doi.org/10.52768/3068-1979/1001
Primary Topic
Neurofibromatosis and Schwannoma Cases
Type
article
Field-Weighted Citation Impact
0.00
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article

A rare case of spinal plexiform neurofibromas in a 9 year old Indian child with Neurofibromatosis Noonan syndrome Clinical and neuroradiological insights

Gulrej Nisar Shaikh
Annals of Pediatrics and Neonatal Care
Neurofibromatosis and Schwannoma Cases
article

A rare case of spinal plexiform neurofibromas in a 9 year old Indian child with Neurofibromatosis Noonan syndrome Clinical and neuroradiological insights

Gulrej Nisar Shaikh
article en

Abstract

Neurofibromatosis Noonan Syndrome (NFNS) is a rare RASopathy resulting from a variant NF1 gene mutation, characterized by a combination of features from both Neurofibromatosis type 1 (NF1) and Noonan Syndrome (NS).

Annals of Pediatrics and Neonatal CareVol. 1(1)
Openalex Percentile: Top 64%
Neurofibromatosis and Schwannoma Cases
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A rare case of spinal plexiform neurofibromas in a 9 year old Indian child with Neurofibromatosis Noonan syndrome Clinical and neuroradiological insights — Gulrej Nisar Shaikh · Annals of Pediatrics and Neonatal Care (2025) | TGRS Research Map | TGRS