Title
A Clinical Guide To Inherited Metabolic Diseases
Delivery time: 8-12 business days (International)
This Userfriendly Clinical Handbook Provides A Clear And Concise Overview Of How To Recognize And Diagnose 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 New Edition Provides More Indepth Coverage On Mitochondrial Disease And Congenital Disorders Of Glycosylation. The Chapters On Neurological Syndrome And Newborn Screening Are Greatly Expanded, As Well As Those On Laboratory Investigation And Treatment.
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⚠️ WARNING (California Proposition 65):
This product may contain chemicals known to the State of California to cause cancer, birth defects, or other reproductive harm.
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Shipping & Returns
Shipping
We ship your order within 2–3 business days for USA deliveries and 5–8 business days for international shipments. Once your package has been dispatched from our warehouse, you'll receive an email confirmation with a tracking number, allowing you to track the status of your delivery.
Returns
To facilitate a smooth return process, a Return Authorization (RA) Number is required for all returns. Returns without a valid RA number will be declined and may incur additional fees. You can request an RA number within 15 days of the original delivery date. For more details, please refer to our Return & Refund Policy page.
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We provide a 2-year limited warranty, from the date of purchase for all our products.
If you believe you have received a defective product, or are experiencing any problems with your product, please contact us.
This warranty strictly does not cover damages that arose from negligence, misuse, wear and tear, or not in accordance with product instructions (dropping the product, etc.).
Warranty
We provide a 2-year limited warranty, from the date of purchase for all our products.
If you believe you have received a defective product, or are experiencing any problems with your product, please contact us.
This warranty strictly does not cover damages that arose from negligence, misuse, wear and tear, or not in accordance with product instructions (dropping the product, etc.).
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Your payment information is processed securely. We do not store credit card details nor have access to your credit card information.
We accept payments with :
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Frequently Asked Questions
- Q: What is 'A Clinical Guide to Inherited Metabolic Diseases' about? A: This clinical handbook provides an overview of recognizing and diagnosing inherited metabolic diseases, guiding readers through the diagnostic process from symptom identification to final diagnosis.
- Q: Who is the author of this book? A: The book is authored by Joe T. R. Clarke.
- Q: How many pages does this book contain? A: The book contains a total of 360 pages.
- Q: What is the binding type of this book? A: The book is available in a paperback binding.
- Q: When was the latest edition of this book published? A: The latest edition of the book was published on January 30, 2006.
- Q: What new content does the latest edition include? A: The new edition includes expanded coverage on mitochondrial disease, congenital disorders of glycosylation, neurological syndromes, and newborn screening.
- Q: Is this book suitable for beginners in the field of metabolic diseases? A: Yes, the book is designed to be user-friendly and serves as a clear guide for those new to diagnosing inherited metabolic diseases.
- Q: Does this book cover treatment options for metabolic diseases? A: Yes, it includes sections on laboratory investigations and treatment options for various inherited metabolic diseases.
- Q: Are there illustrations or diagrams in the book? A: While the product details do not specify illustrations, clinical guides typically include diagrams to aid understanding.
- Q: Is this book part of a series or standalone? A: The product details do not indicate whether this book is part of a series; it appears to be a standalone clinical guide.