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Updated: Dec 15, 2025

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PYRC2-Related Hypomyelinating Leukodystrophy: More to This Than Meets the Eye
Jennifer Rakotomamonjy1, Lauren Rylaarsdam2, Alicia Guemez-Gamboa1
1Department of Physiology, Northwestern University, Chicago, IL 60611, USA.
Neuron
|July 10, 2020
Abstract:
Loss-of-function variants in the PYRC2 gene cause hypomyelinating leukodystrophy 10 (HLD10), but the associated pathogenic mechanisms are unknown. In this issue of Neuron, Escande-Beillard et al. (2020) reveal that PYRC2 is a key enzyme for proper brain development and a regulator of glycine homeostasis, uncovering hyperglycinemia as a driver of HLD10 pathogenesis.

