Infantile Monosialoganglioside2 (GM2) Gangliosidosis With Concurrent Bronchopneumonia: An Extraordinary Case of Tay-Sachs Disease

Tay-Sachs disease (TSD) is a rare, fatal neurodegenerative disorder characterized by the deficiency of the enzyme hexosaminidase-A (Hex A), which results in the accumulation of monosialoganglioside2 (GM2) ganglioside within nerve cells, predominantly affecting individuals of Ashkenazi Jewish descent...

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Veröffentlicht in:	Cureus 2024, Vol.16 (1), p.e51797-e51797
Hauptverfasser:	Grezenko, Han, Al-Deir, Shadi S, Eshete, Filagot D, Faran, Nuzhat, Mimms, Ciara S, Ibrahim, Muhammad
Format:	Report
Sprache:	eng
Online-Zugang:	Volltext
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