Anaesthesia management in a patient with a severe biotinidase deficiency for congenital scoliosis repair

A 17 year old female patient with a biotinidase enzyme deficiency, cerebral palsy, aphamis, generalized hyperreflexia and spasticity, epilepsy and mental retardation came for the severe kyphoscoliotic deformity correction. Biotinidase enzyme deficiency is an autosomal recessive disorder with inciden...

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Bibliographic Details
Main Authors: Ebrahim Almasri, Rashad AlQasim, Puja Deshpande
Format: Article
Language:English
Published: Taylor & Francis Group 2016-01-01
Series:Egyptian Journal of Anaesthesia
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1110184915000835