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Book Description
The expert, up-to-date guidance you need to
identify, understand, and treat neurogenetic
disorders in children Written in a readilyaccessible, highly-readable style, this unique
reference offers a sound starting point and
clinical step-by-step approach to treating the
complex and often baffling neurogenetic
diseases found in children. Conveniently
organized by age groups from prenatal
diagnosis to neonate to childhood, each
chapter begins by describing symptoms
(similar to the way a patient would present),
and then guides you through confirming the
diagnosis and choosing the appropriate course
of therapy. Completely updated to reflect the
significant advances made following the
discovery of the DNA sequence on the human
genome, the Third Edition of Neurology of
Hereditary Metabolic Diseases of Children
clarifies the complicated genetics and
biochemistry of these illnesses and will prove
to be invaluable to the non-specialist and
specialist alike. New to the Third Edition:
Tables