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Autor:
Devesh Gagan MBBS, MD Pediatrics, Sudesh Kumar MD Pediatrics, Piyali Bhattacharya MD Pediatrics, Simranjit Kaur MBBS, MD Pediatrics
Publikováno v:
Global Pediatric Health, Vol 10 (2023)
Pelizaeus-Merzbacher disease, a rare X-linked recessive disease occurring predominantly in males, is a disorder of proteolipid protein expression in myelin formation in the central nervous system. The disease is clinically manifested by neurodevelopm
Externí odkaz:
https://doaj.org/article/bea89b572bf6431da41a8bd4be19c507
