Ekman-Lobstein syndrome
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- Indbinding:
- Paperback
- Sideantal:
- 68
- Udgivet:
- 9. juli 2018
- Størrelse:
- 150x5x220 mm.
- Vægt:
- 119 g.
- 2-3 uger.
- 16. december 2024
På lager
Forlænget returret til d. 31. januar 2025
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- Adgang til 70.000+ titler
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Ingen binding og kan opsiges når som helst.
- 1 valgfrit digitalt ugeblad
- 20 timers lytning og læsning
- Adgang til 70.000+ titler
- Ingen binding
Abonnementet koster 75 kr./md.
Ingen binding og kan opsiges når som helst.
Beskrivelse af Ekman-Lobstein syndrome
There is no satisfactory therapy for many of the disabling genetic disorders such as Ekman-Lobstein syndrome (osteogenesis imperfecta). However, it is hoped that advances arising from the accumulating research evidence can contribute to improving treatment of such conditions. Therefore, reviewing the literature for the recent research evidence is recommended to improve the therapeutic services for such disorders. The occurrence of Ekman-Lobstein syndrome in Iraq has not been documented. In addition to providing the historical documentation of this syndrome, particularly the early history of its documentation, this book describes a case of Ekman-Lobstein syndrome in an Iraqi patient. This book also reviews the available research evidence which may contribute to improving its treatment.
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