[보안 로그인 하기]
[회원가입]  [ID/PW찾기]
    Management of Genetic Syndromes-4판
Management of Genetic Syn
       판매가 : 325,000325,000
       적립금 : 6,500
       저   자 : Carey
       역   자 :
       출판사 : Wiley
    ISBN(13) : 9781119432678
       발행일 : 2020-09  /   4판   /   페이지
       상품코드 : 27647
       수 량 :
       

Description:


This fourth edition of the book Cassidy’s and Allanson’s Management of Genetic Syndromes will be unchanged in
character but will be current in its content. It will include updated information on identification (including newly-
developed diagnostic criteria), genetic basis and diagnostic testing, and management for each of the 59 included
disorders.
The aims of this book have not changed: to provide a resource on diagnosis, genetic counseling and management for
medical professionals (medical geneticists, genetic counselors, and primary care providers) caring for individuals of
all ages affected by relatively common genetic syndromes. It will continue to exclude traditional metabolic disorders,
which are well-covered in other resources.

The format will remain essentially unchanged, though the editors will once again examine the feasibility of a brief
tabular summary of recommended evaluations at the end of each chapter. (Ideally these concise summaries could be
available and freely accessible online). Again, each chapter will be organized in the same manner and cover the same
general topics. In addition, there will be an increase in the number of disorders slightly to approximately 60 as a
result of new expertise, newly recognized conditions, and conditions whose frequency has recently been recognized to
be higher than previously realized.
더보기

The rationale for a new edition is to assure that information is up to date in the rapidly changing field of medical
genetics and genetic diagnostic testing. The sales figures for the prior editions, and the enthusiasm with which they
were received, indicate that there is a strong need for this book on the topic of managing genetic syndromes. The
relatively recent availability of even more sophisticated molecular diagnostic testing for an exponentially increasing
number of genetic conditions has increased the number of individuals who are identified as having them, and has made
it even more imperative for primary care providers and genetic practitioners to have access to information about their
appropriate management.



1 Aarskog Syndrome

2 Achondroplasia

3 Alagille Syndrome

4 Albinism: Ocular and Oculocutaneous Albinism and Hermansky-Pudlak Syndrome

5 Angelman Syndrome

6 Arthrogryposis

7 ATR-X: α-Thalassemia Mental Retardation-X-Linked

8 Bardet-Biedl Syndrome

9 Beckwith-Wiedemann Syndrome and Hemihyperplasia

10 Cardio-Facio-Cutaneous Syndrome

11 CHARGE Syndrome

12 Coffin-Lowry Syndrome
더보기

13 Coffin-Siris Syndrome

14 Cohen Syndrome

15 Cornelia de Lange Syndrome

16 Costello Syndrome

17 Craniosynostosis Syndromes

18 Deletion 1p36 Syndrome

19 Deletion 4p: Wolf-Hirschhorn Syndrome

20 Deletion 5p Syndrome

21 Deletion 22q11.2 (Velo-Cardio-Facial Syndrome/DiGeorge Syndrome)

22 Deletion 22q13 Syndrome: Phelan-McDermid Syndrome

23 Denys-Drash, Frasier, and WAGR Syndromes (WT1-related Disorders)

24 Down Syndrome

25 Ehlers-Danlos Syndromes

26 Fetal Alcohol Syndrome and Fetal Alcohol Spectrum Disorder

27 Fetal Anticonvulsant Syndrome

28 Fragile X Syndrome and Premutation-Associated Disorders

29 Gorlin Syndrome: Nevoid Basal Cell Carcinoma Syndrome

30 Hereditary Hemorrhagic Telangiectasia

31 Holoprosencephaly

32 Incontinentia Pigmenti

33 Inverted Duplicated Chromosome 15 Syndrome (Isodicentric 15)

34 Kabuki Syndrome

35 47,XXY (Klinefelter Syndrome) and Related X and Y Chromosome Conditions

36 Loeys-Dietz Syndrome

37 Marfan Syndrome

38 Mowat-Wilson Syndrome

39 Myotonic Dystrophy Type 1

40 Neurofibromatosis Type 1

41 Noonan Syndrome

42 Oculo-Auriculo-Vertebral Spectrum

43 Osteogenesis Imperfecta

44 Pallister-Hall Syndrome and Greig Cephalopolysyndactyly Syndrome

45 Pallister-Killian Syndrome

46 Prader-Willi Syndrome

47 Proteus Syndrome

48 PTEN Hamartoma Tumor Syndrome

49 Rett Syndrome

50 Robin Sequence

51 Rubinstein-Taybi Syndrome

52 Silver-Russell Syndrome

53 Smith-Lemli-Opitz Syndrome

54 Smith-Magenis Syndrome

55 Sotos Syndrome

56 Stickler Syndrome

57 Treacher Collins Syndrome and Related Disorders

58 Trisomy 18 and Trisomy 13 Syndromes

59 Tuberous Sclerosis Complex

60 Turner Syndrome

61 Vater/Vacterl Association

62 von Hippel-Lindau Syndrome

63 Williams Syndrome

INDEX
클릭 하시면 에스크로 가입여부를 확인 하실 수 있습니다.