Genetic Counseling / Edition 3

by Walter Fuhrmann, Sabine Kurth-Scherer, Friedrich Vogel

Overview

This third edition of Genetic Counseling has been thoroughly revised to reflect current practice. In particular, the chapter on prenatal diagnosis (Chapter 10) has been largely rewritten and considerably expanded, reflecting the rapid development in this field and its increasing medical importance. This chapter provides a detailed description of the alpha-fetoprotein test and a brief description of ultrasonography for the diagnosis of morphologic defects. Further, we discuss fetoscopy and the sampling of fetal blood with the aid of a fetoscope. In this as in past editions, these descriptions are not meant as working instructions for actual practice, but rather as background for the general practitioner who is dealing with the problems of genetic counseling. We have added a chapter (Chapter 7) on the use of conditional probability (Bayes Principle) for the calculation of more exact specific risk figures. It is true that the daily practice of medicine sees far fewer situations in which these methods can reasonably be applied than some theoreticians like to think. However, the usefulness of these methods has recently increased, especially in cases of X-chromosomal recessive diseases where the termination of a preg­ nancy, if the fetus has been ascertained to be male and if the mother is "most probably" heterozygous, has become more commonplace. With such a trend, the degree of probability must be determined as exactly as possible.

Product Details

ISBN-13:	9780387907154
Publisher:	Springer New York
Publication date:	11/04/1982
Edition description:	3rd ed. 1983
Pages:	188
Product dimensions:	6.10(w) x 9.25(h) x (d)

Table of Contents

1 Appearances Deceive.- 2 Recording a Family Medical History or Pedigree.- 3 The Autosomal Dominant Mode of Inheritance.- 4 New Mutations and Nonhereditary Cases (Phenocopies and Somatic Mutations).- 5 The Autosomal Recessive Mode of Inheritance and Tests for the Detection of Heterozygotes.- 6 Sex-Linked Modes of Inheritance.- 7 How Can Additional Information Be Incorporated into Genetic Risk Calculations?.- 8 Chromosomal Aberrations.- 9 Malformations Not Subject to a Simple Mode of Inheritance.- 10 Prenatal Diagnosis of Genetic Abnormalities and Diseases.- 11 Other Diseases Without a Simple Mode of Inheritance.- 12 Mental Retardation and Mental Illness.- 13 Genetic Prognosis for a Consanguineous Marriage.- 14 Exposure to Mutagenic Noxes.- 15 Teratogenic Effects During Early Pregnancy.- 16 Psychological and Social Considerations.- References.