Hughes Syndrome (PDF)
The second edition of Hughes Syndrome: Antiphospholipid Syndrome addresses the complete range of conditions produced by this common disorder which is also known as APS or "sticky blood" syndrome. APS is one of the main causes of strokes (40%), leg deep...
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The second edition of Hughes Syndrome: Antiphospholipid Syndrome addresses the complete range of conditions produced by this common disorder which is also known as APS or "sticky blood" syndrome. APS is one of the main causes of strokes (40%), leg deep vein thrombosis, and recurrent miscarriages in women. It is an important risk factor for thrombosis in women taking the oral contraceptive pill.
The effects of this syndrome were found initially in thrombosis, obstetrics (APS is the most common treatable cause of recurrent pregnancy loss) and neurology. Its impact is now felt in a diverse range of conditions. These include surgery (graft rejection), orthopedics (avascular necrosis, DVT), psychiatry (memory loss), cardiology (pulmonary hypertension, valvular disease, angina), ENT (vertigo), pediatrics (young strokes, epilepsy) to name but a few.
This new and updated text reflects the growth in published literature on APS and the widening ramifications of the disease. APS is a multi-specialty disease and is of increasing interest to obstetricians, rheumatologists, hematologists, dermatologists, neurologists and immunologists.
- 2006, 2nd ed. 2006, 598 Seiten, Englisch
- Herausgegeben: Munther A Khamashta
- Verlag: Springer-Verlag GmbH
- ISBN-10: 1846280095
- ISBN-13: 9781846280092
- Erscheinungsdatum: 15.06.2006
Abhängig von Bildschirmgröße und eingestellter Schriftgröße kann die Seitenzahl auf Ihrem Lesegerät variieren.
- Dateiformat: PDF
- Größe: 6.06 MB
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"The order in which the topics are arranged is very practical. The high quality photographic figures with captions are informative and visually appealing. I like artwork on the hardbound cover. This book appears to be well-written and well-organized. It is a useful addition to my library, both for its content and as a thorough database of references on the topic of Hughes syndrome. Given the ongoing research and development of new knowledge in this field, the second edition is a welcome update." (Cory B Pittman, Doody Enterprises, Inc. - COPYRIGHT 2006)
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