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March 25, 2026Annals of Child NeurologyOpen Access

A Neonate with a Recurrent 16p12.2 Microdeletion Presenting with Hypotonia and Feeding Difficulty: A Case Report

Jun Chul Byun Chun Soo Kim Kyungbo Kim

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Key Points

This research aims to describe the clinical features and implications of a recurrent 16p12.2 microdeletion in a neonate.
Detailed clinical assessment of a neonate with hypotonia and feeding difficulties
Chromosomal microarray analysis performed to identify genetic abnormalities
Case review and approval obtained from relevant medical authorities
Identification of a 909 kb recurrent 16p12.2 microdeletion
Neonate exhibited significant hypotonia and feeding challenges
Clinical features aligned with known outcomes of 16p12.2 microdeletions

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Implication

Case reports recurrent 16p12.2 microdeletion associated with feeding challenges in a neonate, suggesting broader diagnostic guidelines.

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Cite This Study

Byun et al. (2026) studied this question.

synapsesocial.com/papers/69c770c08bbfbc51511e0c4d https://doi.org/10.26815/acn.2025.01277

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Synapse has enriched 10 related papers. Consider them for comparative context:

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