Fragile X Syndrome: From Diagnosis to Treatment - ein Angebot gefunden
Bester Preis: € 96,44 (vom 04.05.2022)Aus dem Archiv:
1
Fragile X Syndrome: From Diagnosis to Treatment
EN NW EB DLISBN: 9781685075934 bzw. 1685075932, in Englisch, Nova Science Publishers, Inc. neu, E-Book, elektronischer Download.
Lieferung aus: Vereinigtes Königreich Großbritannien und Nordirland, Despatched same working day before 3pm.
Fragile X syndrome is an inherited disease caused by an excessive length of the FMR protein due to mutations in the FMR1 gene located on the X chromosome.It is commonly described as one of the most common genetic diseases with autism-like behaviors and related developmental disabilities.Beside intellectual delays, behavioral problems, and communication difficulties, mood disorders usually occur.Diagnosis is based on laboratory tests and DNA results.Phenotypes including long and narrow face, large ears, hyper-arched palate, flat feet, ataxia, seizures, anxiety, aggression, and hand-related stereotypic behaviors are frequently observed.Although there is no specific cure, early interventions are highly encouraging, promising, and recommended.Pharmacological treatments may be combined with behavioral and/or cognitive behavioral interventions.Recently, assistive technology-based programs have been implemented.This volume includes seven chapters and addresses the newest advances in the diagnosis and treatment of individuals with Fragile X syndrome.Chapter One encompasses the molecular features and pathological bases of the disease.A comprehensive literature overview was conducted. The role of the FMR protein was emphasized although few studies evaluated its function.Chapter Two deals with the neuropsychiatric symptoms related to the syndrome.A complete conceptual framework was exhaustively detailed.Chapter Three emphasizes the role of pharmacotherapy in the treatment of Fragile X syndrome.A further literature review was carried out. Clinical relevance was outlined. Chapter Four provides the reader with a conceptual analysis.Besides molecular features, brain development was described.Challenging behaviors were included and the importance of the early combined intervention was critically discussed.Chapters Five, Six, and Seven detailed three case reports on the effectiveness and the suitability of assistive technology-based interventions.Specifically, Chapter Five argued for microswitch-cluster technology focused on pursuing the dual simultaneous goal of promoting an adaptive response (i.e., object manipulation) and reducing a challenging behavior (i.e., hand mouthing).Chapter Six describes a combined microswitch and VOCA program useful to ensure the participant has the choice between independent access to positive stimulation and asking for social interaction.Finally, Chapter Seven includes choice opportunities through an assistive technology-mediated program involving a boy with Fragile X in a functional task.Targeted readers (i.e., caregivers, clinicians, speech therapists, professionals, psychologists, neurologists, parents of children with Fragile X syndrome, teachers) may find interesting and stimulating tips and insights for daily use in clinical research and practice, with the dual objective of diagnosis and treatment.
Fragile X syndrome is an inherited disease caused by an excessive length of the FMR protein due to mutations in the FMR1 gene located on the X chromosome.It is commonly described as one of the most common genetic diseases with autism-like behaviors and related developmental disabilities.Beside intellectual delays, behavioral problems, and communication difficulties, mood disorders usually occur.Diagnosis is based on laboratory tests and DNA results.Phenotypes including long and narrow face, large ears, hyper-arched palate, flat feet, ataxia, seizures, anxiety, aggression, and hand-related stereotypic behaviors are frequently observed.Although there is no specific cure, early interventions are highly encouraging, promising, and recommended.Pharmacological treatments may be combined with behavioral and/or cognitive behavioral interventions.Recently, assistive technology-based programs have been implemented.This volume includes seven chapters and addresses the newest advances in the diagnosis and treatment of individuals with Fragile X syndrome.Chapter One encompasses the molecular features and pathological bases of the disease.A comprehensive literature overview was conducted. The role of the FMR protein was emphasized although few studies evaluated its function.Chapter Two deals with the neuropsychiatric symptoms related to the syndrome.A complete conceptual framework was exhaustively detailed.Chapter Three emphasizes the role of pharmacotherapy in the treatment of Fragile X syndrome.A further literature review was carried out. Clinical relevance was outlined. Chapter Four provides the reader with a conceptual analysis.Besides molecular features, brain development was described.Challenging behaviors were included and the importance of the early combined intervention was critically discussed.Chapters Five, Six, and Seven detailed three case reports on the effectiveness and the suitability of assistive technology-based interventions.Specifically, Chapter Five argued for microswitch-cluster technology focused on pursuing the dual simultaneous goal of promoting an adaptive response (i.e., object manipulation) and reducing a challenging behavior (i.e., hand mouthing).Chapter Six describes a combined microswitch and VOCA program useful to ensure the participant has the choice between independent access to positive stimulation and asking for social interaction.Finally, Chapter Seven includes choice opportunities through an assistive technology-mediated program involving a boy with Fragile X in a functional task.Targeted readers (i.e., caregivers, clinicians, speech therapists, professionals, psychologists, neurologists, parents of children with Fragile X syndrome, teachers) may find interesting and stimulating tips and insights for daily use in clinical research and practice, with the dual objective of diagnosis and treatment.
Kategorie: School & Text Books, Education > Society & social sciences > Teaching of specific groups & persons with special education, ebooks > School & Text Books
Daten vom 04.05.2022 03:51h
ISBN (andere Schreibweisen): 1-68507-593-2, 978-1-68507-593-4
Daten vom 04.05.2022 03:51h
ISBN (andere Schreibweisen): 1-68507-593-2, 978-1-68507-593-4
Zuerst gefunden: 04.05.2022 03:51:17
Zuletzt gefunden: 04.05.2022 03:51:17
Kleinster Preis: € 96,44 (vom 04.05.2022 03:51:17)
Höchster Preis: € 96,44 (vom 04.05.2022 03:51:17)
Fundstellen insgesamt: 1
Zuletzt gefunden: 04.05.2022 03:51:17
Kleinster Preis: € 96,44 (vom 04.05.2022 03:51:17)
Höchster Preis: € 96,44 (vom 04.05.2022 03:51:17)
Fundstellen insgesamt: 1
Momentan keine Suchergebnisse - vielleicht bald lieferbar
Ihre Suche nach ist bei mehr als 100 angebundenen Webshops momentan nicht lieferbar. Wir finden dieses Buch aber trotzdem innerhalb weniger Wochen.
Sie Suchen nach diesem Buch:Fabrizio Stasolla: Fragile X Syndrome: From Diagnosis to Treatment
ISBN: 9781685075934
Speichern Sie diese Suche kostenlos in ab, dann werden Sie automatisch benachrichtigt, sobald dieses Buch verfügbar ist. Meistens finden wir dieses Buch innerhalb weniger Wochen und verständigen Sie dann per E-Mail. Sie können dann frei entscheiden, ob Sie das Buch kaufen wollen oder nicht.
Unsere Suchtipps für Ihre Suche:
- Alle Bücher des Autors.: Suche nach "Autor: fabrizio stasolla" liefert mehr Ergebnisse
- Suchen nach Suchbegriffen wie Autor oder Titel des Buches sind erfolgreicher als solche nach der ISBN.: Suche nach "diagnosis treatment syndrome fabrizio stasolla" liefert mehr Ergebnisse
Sie haben jetzt folgende Möglichkeiten:
- Speichern Sie diese Seite in Ihren Lesezeichen oder Favoriten ab, dann können Sie jederzeit die Suche erneut ausführen.
- Das Buch ist tatsächlich derzeit vergriffen bzw. nicht lieferbar. Es ist z.B. eine Rarität. Möglicherweise ist es aber in einiger Zeit lieferbar. Speichern Sie dazu diese Suche kostenlos ab oder lassen Sie sich kostenlos auf dieses Gerät benachrichten und Sie werden automatisch per E-Mail oder Nachricht informiert, sobald dieses Buch wieder lieferbar wird. Wir sind zuversichtlich, dass wir jedes Buch auf diese Weise innerhalb relativ kurzer Zeit finden. Probieren Sie es einfach aus!
Mich bei neuen Ergebnissen benachrichtigenSuche jetzt kostenlos SpeichernIn 50 Millionen auch bereits vergriffenen Büchern recherchieren!
Anmeldung mit Google:
ODER
Anmeldung mit Facebook:
Lade…