Complex Glycerol Kinase Deficiency (Xp21 Deletion Syndrome): A Case Report of a Contiguous Gene Disorder Necessitating Creative Anesthetic Planning

Rossell, B; Godart, J; Petyt, C; Veyckemans, F

Veyckemans, F (corresponding author), Hop Jeanne Flandre, Serv Anesthesie Reanimat Pediat, Ave Eugene Avinee, F-59037 Lille, France.

A & A PRACTICE, 2020; 14 (10):

Abstract

We report a case of Xp21 deletion syndrome, a contiguous gene syndrome associating glycerol kinase deficiency, Duchenne muscular dystrophy, and congen......

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