ABSTRACT

Inherited Metabolic Diseases are common enough for health, social service and education professionals to encounter them periodically, but rare enough for them to be poorly understood. They severely affect up to 1 in 10,000 people, and lead to a wide range of special needs in care and education. This guide provides specialist information on metabolic diseases for the non-specialist. In a concise, accessible and family-friendly format, each entry lists the names by which a condition is known, and explains the genetic causes of the disease, the physical effects, the patient's symptoms, and available treatments. Key diseases from all ten major groups of metabolic disorders are described, and all entries have been reviewed by Specialist Advisers. The work has been coordinated by the charity Climb, Children Living with Inherited Metabolic Diseases. This uniquely comprehensive source of information is a vital reference for hospital doctors including paediatricians, general practitioners, nurses and other health professionals, social service and education staff and managers, and the families and carers of children with the conditions.

chapter 3|17 pages

Mitochondrial and peroxisomal disorders

chapter 4|16 pages

Lysosomal, sterol and lipid disorders

chapter 5|13 pages

Carbohydrate and glycosylation disorders

chapter 6|13 pages

Purine, pyrimidine and porphyria disorders

chapter 7|14 pages

Hormone disorders

chapter 9|16 pages

Blood and immune system disorders

chapter 10|16 pages

Associated disorders