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This groundbreaking new text explains and documents the scientific
basis of chronic pain in Joint Hypermobility Syndrome (JHS) and
other heritable disorders of connective tissue from the
physiological, epidemiological, genetic and clinical viewpoints. It
asks the reader to consider the possibility of JHS, identify it
clinically, understand its co-morbidities, including
interdependencies with Fibromyalgia and Chronic Fatigue Syndrome,
while managing the condition appropriately. Hypermobility,
Fibromyalgia and Chronic Pain takes a multi-specialty and
multidisciplinary approach to understanding JHS and its management,
drawing together expertise from a broad group of
internationally-recognized authors. The book is split into two
sections. Section 1 deals with the clinical manifestations of JHS
and Fibromyalgia, their epidemiology and pathophysiology. Section 2
covers clinical management. Here the reader will find chapters
covering pharmacotherapeutics, psychotherapy and physical therapies
that address the needs of patients from childhood to adulthood. It
is hoped that Hypermobility, Fibromyalgia and Chronic Pain will
advance knowledge of therapies and provoke further research while
stimulating interest and encouraging debate. Comprehensively
relates practical therapy to the nature of the underlying pathology
Covers in one single text both the scientific and practical
management aspect of Joint Hypermobility Syndrome and its allied
pathologies Contributions from over 30 leading international
experts Multidisciplinary approach will support all health
professionals working in this field
Following a brief description of the historical and genetic
background of the condition HMS is described in relation to other
connective tissue disorders, such as Ehlers-Danlos syndrome, the
Marfan Syndrome etc. The hypermobility syndrome is distinct from
hypermobility (as in one joint only), which most physiotherapists
are familiar with, and this difference will be explored.
Hypermobility, is something people are born with, but it does not
necessarily produce symptoms. It is present in between 5-15% of the
population. Many of these will suffer symptoms at some stage in
their life. It may occur in childhood, adolescence, adulthood,
pregnancy or old age. Each of these stages is covered in the book,
with detailed information on the presentation of the condition and
its management. There are contributions from a variety of medical
practitioners experienced in this field:. Consultant
Rheumatologist, Professor R Grahame, Consultant Paediatrician, Dr K
Murray, GP, Dr E Mansi, several physiotherapists, who specialise in
different areas; Rosemary Keer (adults), Alison Middleditch
(adolescents), Vicky Harding (Chronic pain), Jane Simmonds
(Rehabilitation) & Sue Maillard (paediatric). There will also
be a contribution from Sarah Gurley-Green, past Chairperson to the
Hypermobility Syndrome association. Demonstrates how to identify
the condition in the clinic. Discusses treatment and management
strategies. Provides examples in the form of case studies. Includes
details of a comprehensive assessment procedure, which differs
depending on the stage of the disorder and the age of the patient.
Features contributions by experts in a range of medical fields.
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