Sanjad-Sakati-Richardson-Kirk syndrome
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- Indbinding:
- Paperback
- Sideantal:
- 56
- Udgivet:
- 10. januar 2019
- Størrelse:
- 150x4x220 mm.
- Vægt:
- 102 g.
- 2-3 uger.
- 16. december 2024
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Forlænget returret til d. 31. januar 2025
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- 1 valgfrit digitalt ugeblad
- 20 timers lytning og læsning
- Adgang til 70.000+ titler
- Ingen binding
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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 Sanjad-Sakati-Richardson-Kirk syndrome
The syndrome of severe growth retardation , mental retardation, and chronic hypocalcemia caused by hypoparathyroidism was first reported by Sanjad, Sakati, and Abu-Osba in 1988. However, the syndrome was first fully described in 1990 by Ricky J Richardson from the Sick Children Hospital of Great Ormond Street in London, and Jeremy MW Kirk from St Bartholomew's Hospital in London. Richardson and Kirk emphasized that this association of a previously undescribed congenital anomalies represented a new syndrome that was observed in eight children of middle eastern origin. They thought that early recognition of this rare disorder may decrease the associated morbidity and mortality. The total number of the reported patients with Sanjad-Sakati-Richardson-Kirk syndrome is 103. Sanjad-Sakati-Richardson-Kirk syndrome has not been reported before in Iraq. The main aim of this book is to describe the first case of this syndrome in Iraq which is the case number 104 in the world.
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