The Chromosome 22q11.2 Deletion Syndrome by McDonald-McGinn, Donna M.;

A Multidisciplinary Approach to Diagnosis and Treatment

10% KEDVEZMÉNY?
A kedvezmény csak az 'Értesítés a kedvenc témákról' hírlevelünk címzettjeinek rendeléseire érvényes.

Kiadói listaár EUR 132.00
Az ár azért becsült, mert a rendelés pillanatában nem lehet pontosan tudni, hogy a beérkezéskor milyen lesz a forint árfolyama az adott termék eredeti devizájához képest. Ha a forint romlana, kissé többet, ha javulna, kissé kevesebbet kell majd fizetnie.

51 559 Ft (49 104 Ft + 5% áfa)
Kedvezmény(ek) 10% (cc. 5 156 Ft off)
Kedvezményes ár 46 403 Ft (44 194 Ft + 5% áfa)

51 559 Ft

Beszerezhetőség

Megrendelésre a kiadó utánnyomja a könyvet. Rendelhető, de a szokásosnál kicsit lassabban érkezik meg.

A termék adatai:

Kiadó Elsevier Science
Megjelenés dátuma 2022. augusztus 24.

ISBN 9780128160473
Kötéstípus Puhakötés
Terjedelem524 oldal
Méret 234x190 mm
Súly 1040 g
Nyelv angol

Kategóriák

A biológia általános kérdései Genetika, evolúció, fejlődéstan Genetika A biológia általános kérdései (karitatív célú kampány) Genetika, evolúció, fejlődéstan (karitatív célú kampány) Genetika (karitatív célú kampány)

Hosszú leírás:

The Chromosome 22q11.2 Deletion Syndrome: A Multidisciplinary Approach to Diagnosis and Treatment serves as the first comprehensive, user-friendly resource on the etiology, prognosis, and recurrence risk associated with the chromosome 22q11.2 deletion syndrome. Leading international contributors cover the background, genetics, testing methods, and pathophysiology of 22q11.2DS, placing emphasis on a strong foundation for multidisciplinary treatment strategies. Written by specialists in every applicable subspecialty, such as, cardiology, immunology, endocrinology, gastroenterology, hematology, ophthalmology, neurology, and psychiatry, among other fields. This book presents an authoritative resource with full color images that enhance concept illustration and aid in real-time decision-making.

As 22q11.2 deletion syndrome has become a model for understanding rare and frequent anomalies, numerous medical issues, cognitive and behavioral phenotypes, and later onset conditions, this text will become the go to resource for clinicians, researchers, trainees, and motivated family members, in gaining a full understanding of this complex chromosomal disorder.

Több

Tartalomjegyzék:

1. 22q11.2 deletion syndrome: Setting the stage
2. Genetics, mechanism, and pathophysiology of 22q11.2 deletion syndrome
3. Embryonic development in 22q11.2 deletion syndrome
4. Congenital heart disease and cardiovascular abnormalities associated with 22q11.2 deletion syndrome
5. The immune system in 22q11.2 deletion syndrome
6. Craniofacial abnormalities in association with 22q11.2 deletion syndrome
7. Otolaryngologic issues in association with 22q11.2 deletion syndrome
8. Endocrine features of 22q11.2 deletion syndrome
9. Gastroenterological manifestations associated with 22q11.2 deletion syndrome
10. Genitourinary abnormalities in association with 22q11.2 deletion syndrome
11. Hematologic and oncological manifestations of 22q11.2 deletion syndrome
12. Skeletal anomalies associated with 22q11.2 deletion syndrome
13. Ocular findings in 22q11.2 deletion syndrome
14. Neurological features associated with 22q11.2 deletion syndrome
15. Neurodevelopmental outcome, developmental trajectories, and management in 22q11.2 deletion syndrome
16. Speech and language manifestations in 22q11.2 deletion syndrome
17. Psychiatric profile in children and youth with 22q11.2 deletion syndrome
18. Mental health in adults with 22q11.2 deletion syndrome
19. Primary pediatric care for children and youth with 22q11.2 deletion syndrome
20. Healthcare transitions for adolescents and adults with 22q11.2 deletion syndrome
21. Reproduction, prenatal screening, and diagnosis in 22q11.2 deletion syndrome
22. Quality of life: Educational, vocational, and life planning for individuals with 22q11.2 deletion syndrome
23. 22q11.2 deletion syndrome: Future directions
24. General management principles for 22q11.2 deletion syndrome
25. Medical needs associated with 22q11.2 deletion syndrome