"Will Larson's An Elegant Puzzle orients around the particular challenges of engineering management--from sizing teams to technical debt to succession planning--and provides a path to the good solutions. Drawing from his experience at Digg, Uber, and Stripe, Will Larson has developed a thoughtful ap
Recognition and management of childhood cancer syndromes: A systems approach
✍ Scribed by Clericuzio, Carol L.
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 44 KB
- Volume
- 89
- Category
- Article
- ISSN
- 0148-7299
- DOI
- 10.1002/(sici)1096-8628(19990625)89:2<81::aid-ajmg5>3.0.co;2-i
No coin nor oath required. For personal study only.
✦ Synopsis
Recognition of congenital anomalies that predispose to childhood cancer allows for the institution of a cancer surveillance program, identification of relatives with increased cancer risk, and recurrence risk counseling. In this article, a systems approach to the diagnosis of 21 childhood cancer syndromes is set forth in the format of the pediatric physical examination. In the second part of this article, guidelines are presented for genetic testing, cancer screening, and genetic counseling for the 21 cancer syndromes. Am.
📜 SIMILAR VOLUMES
Comment concevoir et accompagner les changements dans une organisation pour la rendre plus performante ? Depuis une vingtaine d’années, le management s’enrichit d’approches qui s’intéressent aux modes de fonctionnement des systèmes, à la manière de résoudre les problèmes, à l’intelligence collective
Williams syndrome is a genetic disorder linked to cognitive and behavioral patterns of varying consistency; this study was conducted to clarify further the strengths and weaknesses of children with Williams syndrome. Fifteen subjects with the characteristic features of Williams syndrome were evaluat
The essential guide to diagnosis, treatment and management of the various forms of cancer.Cancer is a word filled with foreboding, but this marvellous book by two of our most distinguished oncologists explains its mysteries in lucid, straightforward language that allays fears and puts the disease cl
Five boys and two girls from a large consanguineous British Muslim family of Pakistani origin are described. All presented from infancy to early childhood with progressive moderate to severe developmental delay, postnatal microcephaly, spastic quadriplegia, refractory seizures, and visual handicap.