Zobrazeno 1 - 2
of 2
pro vyhledávání: '"H.S. Meghavathi"'
Publikováno v:
Global Medical Genetics, Vol 10, Iss 02, Pp 105-108 (2023)
Congenital disorder of glycosylation (CDG) is an autosomal recessively inherited disorder. Hypotonia, stroke-like episodes, and peripheral neuropathy are also associated with the condition that typically develops during infancy. The patient, a 12-yea
Externí odkaz:
https://doaj.org/article/2b66589928614bfc8e5ed01baa054e8d
Publikováno v:
Pain & Central Nervous System Week; 6/23/2023, p161-161, 1p