Beckwith Wiedemann syndrome - Al Mosawi, Aamir
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Early recognition of rare hereditary syndromes can be vital. Early recognition of some rare syndromes may allow the anticipation of potentially harmful complications and reducing its damaging consequences. Early diagnosis of rare hereditary disorders also facilitates the provision of early genetic counseling which might contribute to preventing further cases which are expected to have a negative impact on the family. The occurrence of Beckwith Wiedemann syndrome in Iraq has not been reported or documented. In addition, to providing the historical documentation of this syndrome, particularly…mehr

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Produktbeschreibung
Early recognition of rare hereditary syndromes can be vital. Early recognition of some rare syndromes may allow the anticipation of potentially harmful complications and reducing its damaging consequences. Early diagnosis of rare hereditary disorders also facilitates the provision of early genetic counseling which might contribute to preventing further cases which are expected to have a negative impact on the family. The occurrence of Beckwith Wiedemann syndrome in Iraq has not been reported or documented. In addition, to providing the historical documentation of this syndrome, particularly the early history of its documentation during the 1946s, 1970s, and 1980s, this book describes the first case of this rare syndrome in Iraq.
Autorenporträt
Aamir Jalal Al Mosawi is advisor in pediatrics and pediatric psychiatry at the Children Teaching Hospital of Baghdad Medical City. He is the Head of Iraq Headquarter of Copernicus Scientists International Panel. He also served as a member of the advisory council the International Association of Medical Colleges (IAMC).