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A case of type II fucosidosis-diagnosed with neuroradiological and dysmorphological findings

Sanjay M Khaladkar1, Satvik Dhirawani1, Aastha Agarwal1

  • 1Department of Radiodiagnosis, Dr. D. Y. Patil Medical College and Research Centre, Pune, Maharashtra, India.

Current Journal of Neurology
|March 1, 2024
PubMed
Abstract

No abstract available in PubMed .

Keywords:
Inborn Errors of MetabolismLysosomal Storage DiseasesMagnetic Resonance ImagingNeurologyPediatrics

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Lysosomal Hydrolases01:22

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Lysosomes are the site for the degradation of macromolecules and biological polymers released during membrane trafficking events such as secretory, endocytic, autophagic, and phagocytic pathways. The membrane-enclosed area of the lysosome, called the lumen, contains hydrolytic enzymes active in an acidic environment. These acid hydrolases are functional at a pH between 4.5 and 5 and are involved in cellular processes such as cell signaling, energy metabolism, restoration of the plasma membrane,...

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