Inicio > Economía, finanzas, empresa y gestión > Empresa y gestión > Deficiência de glicose 6 fosfato desidrogenase
Deficiência de glicose 6 fosfato desidrogenase

Deficiência de glicose 6 fosfato desidrogenase

Ines Maaloul

65,61 €
IVA incluido
Disponible
Editorial:
KS OmniScriptum Publishing
Año de edición:
2025
Materia
Empresa y gestión
ISBN:
9786209118579
65,61 €
IVA incluido
Disponible

Selecciona una librería:

  • Librería Samer Atenea
  • Librería Aciertas (Toledo)
  • Kálamo Books
  • Librería Perelló (Valencia)
  • Librería Elías (Asturias)
  • Donde los libros
  • Librería Kolima (Madrid)
  • Librería Proteo (Málaga)
Sobre IBD

A deficiência de G6PD é uma das doenças genéticas mais difundidas no mundo, afectando mais de 400 milhões de pessoas, principalmente da bacia do Mediterrâneo. Sendo uma doença ligada ao X, afecta principalmente os rapazes, embora as raparigas também possam ser afectadas (mutações de novo). A OMS classificou a deficiência em 3 classes. As deficiências das classes 2 e 3 caracterizam-se por um risco de choque hemolítico agudo na sequência de stress oxidativo.Fora do episódio agudo, o tratamento baseia-se em medidas preventivas, evitando medicamentos e alimentos que possam precipitar uma crise de hemólise intravascular.

Artículos relacionados

  • Managing TrumPolitical Projects
    Yasser Osman
    Corrupt politicians and businessmen have been using construction projects to funnel money to secret projects since the first iron shovels broke ground. Yet today, throughout the world, there is little if any protection from it. In many countries, governments themselves don’t just ignore these affairs. They sponsor them.Individual project managers – hired to manage a project’s o...
    Disponible

    14,97 €

  • Climbing The Ladder
    Delroy Constantine-Simms
    Climbing The Ladder is an introductory book to mentoring, for organizational decision makers, that may be considering, the feasibility of maintaining, adopting and diversify their organizational mentoring strategies.Most importantly, the author explains that mentoring can take the form of a one-time intervention or a lifelong partnership, which can be a formal structured progra...
    Disponible

    96,53 €

  • The Gen-Savvy Financial Advisor
    Cam Marston
    There have been big changes in consumers’ buying habits, and financial services are no exception, says Cam Marston, a world-renowned expert on generational issues in the marketplace. Understanding clients’ age-based points of view is an indispensable soft skill that you can use to establish connections and make sales. New attitudes about investing break down along generationa...
    Disponible

    14,82 €

  • Your First Job
    Mark Blayney
    Each year in the UK approximately half a million young people enter the world of work for the first time and begin to compete in their careers.And how well you cope with the pressures and demands of your first year of work can help determine how successful a career you will go on to have, and how far you will reach.But with Your First Job, you can get an unfair advantage over y...
    Disponible

    7,82 €

  • Successful Customer Relationship Management Programs and Technologies
    Riyad Eid
    The field of Customer Relationship Management (CRM) has broadened greatly in recent years as technological applications have expanded. Successful Customer Relationship Management Programs and Technologies: Issues and Trends offers the latest research and developments for researchers, practitioners, and academics alike. This volume contains case studies, methodologies, framework...
  • Feral Information Systems Development
    Kerr
    Management invests in large information systems in order to improve the effectiveness of their organization. However, when these systems fail to meet the needs of organizational employees, feral information systems (FIS) are created in order to assist workers with their jobs or to avoid existing organizational information systems. Feral Information Systems Development: Manageri...

Otros libros del autor

  • Carenza di glucosio 6-fosfato deidrogenasi
    Ines Maaloul
    Il deficit di G6PD è una delle malattie genetiche più diffuse al mondo, che colpisce più di 400 milioni di persone, soprattutto del bacino del Mediterraneo. Essendo una malattia legata all’X, colpisce principalmente i maschi, sebbene anche le femmine possano esserne affette (mutazioni de novo). L’OMS ha classificato la carenza in 3 classi. Le carenze di classe 2 e 3 sono caratt...
    Disponible

    65,55 €

  • Niedobór dehydrogenazy glukozo-6-fosforanowej
    Ines Maaloul
    Niedobór G6PD jest jednym z najbardziej rozpowszechnionych zaburzeń genetycznych na świecie, dotykającym ponad 400 milionów ludzi, głównie z basenu Morza Śródziemnego. Jako choroba sprzężona z chromosomem X, dotyka głównie chłopców, chociaż może również dotyczyć dziewcząt (mutacje de novo). WHO sklasyfikowała niedobór w 3 klasach. Niedobory klasy 2 i 3 charakteryzują się ryzyki...
    Disponible

    65,61 €

  • Der Glukose-6-Phosphat-Dehydrogenase-Mangel
    Ines Maaloul
    Der G6PD-Mangel ist eine der weltweit am weitesten verbreiteten genetischen Erkrankungen, von der über 400 Millionen Menschen betroffen sind, vor allem aus dem Mittelmeerraum. Da es sich um eine X-chromosomale Krankheit handelt, sind vor allem Jungen betroffen, aber auch Mädchen können betroffen sein (de novo-Mutationen). Die WHO hat den Mangel in drei Klassen eingeteilt. Die D...
    Disponible

    65,61 €

  • Glucose 6 phosphate dehydrogenase deficiency
    Ines Maaloul
    G6PD deficiency is one of the most widespread genetic disorders in the world, affecting over 400 million people, mainly from the Mediterranean basin. Being an X-linked disease, it mainly affects boys, although girls can also be affected (de novo mutations). The WHO has classified the deficiency into 3 classes. Class 2 and 3 deficiencies are characterized by a risk of acute hemo...
    Disponible

    65,49 €

  • Le syndrome de Wiskott Aldrich
    Ines Maaloul
    Le syndrome de wiskott aldrich (SWA) est un déficit immunitaire rare lié à X, caractérisé par des mutations du gène WAS. Il se manifeste cliniquement par une triade : l’hémorragie conséquence de la thrombopénie, les infections à répétitions et de l’eczéma. Le séquençage génétique est l’examen de confirmation du SWA. La greffe des cellules souches et la thérapie génique sont des...
    Disponible

    66,66 €

  • Le syndrome d’Omenn
    Ines Maaloul
    Le syndrome d’Omenn est une forme rare de déficit immunitaire comboné sévère à transmission autosomique récessive. Il a été décrit pour la première fois par Gilbert S Omenn en 1965. Il associe des infections récurrentes, une érythrodermie ichtyosiforme, une éosinophilie, une lymphadénopathie et une hépatosplénomégalie, accompagnées de symptômes respiratoires, gastro-intestinaux...
    Disponible

    66,66 €