A Clinical Guide to Inherited Metabolic Diseases

This user-friendly clinical handbook provides an overview of how to go about recognizing and diagnosing inherited metabolic diseases.

Joe T. R. Clarke (Author)

9780521614993, Cambridge University Press

Paperback, published 8 December 2005

360 pages, 60 b/w illus.
24.7 x 17.1 x 1.9 cm, 0.57 kg

'… excellent and very readable book … The concise but comprehensive nature of this book makes it a must have on the book shelf for those working in clinical biochemistry. Of all the books on metabolic diseases on my desk this is the one that is always missing!' Human Genetics

This user-friendly clinical handbook provides a clear and concise overview of how to go about recognizing and diagnosing inherited metabolic diseases. The reader is led through the diagnostic process from the identification of those features of an illness suggesting that it might be metabolic through the selection of appropriate laboratory investigation to a final diagnosis. The book is organized into chapters according to the most prominent presenting problem of patients with inherited metabolic diseases: neurologic, hepatic, cardiac, metabolic acidosis, dysmorphism, and acute catastrophic illness in the newborn. It also includes chapters on general principles, laboratory investigation, neonatal screening, and the principles of treatment. This new edition includes much greater depth on mitochondrial disease and congenital disorders of glycosylation. The chapters on neurological syndrome and newborn screening are greatly expanded, as are those on laboratory investigation and treatment, to take account of the very latest technological developments.

Preface to third edition
1. General principles
2. Neurologic syndrome
3. Metabolic acidosis
4. Hepatic syndrome
5. Cardiac syndromes
6. Storage syndromes and dysmorphism
7. Acute metabolic illness in the newborn
8. New born screening
9. Laboratory investigation
10. Treatment
Index.

Subject Areas: Neonatal medicine [MJWN], Paediatric medicine [MJW], Neurology & clinical neurophysiology [MJN], Endocrinology [MJG], Medical genetics [MFN]