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Small Supernumerary Marker Chromosomes (sSMC) - Thomas Liehr

Small Supernumerary Marker Chromosomes (sSMC)

A Guide for Human Geneticists and Clinicians

(Autor)

Buch | Softcover
XX, 220 Seiten
2014 | 2012
Springer Berlin (Verlag)
978-3-642-43536-2 (ISBN)
CHF 119,80 inkl. MwSt
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With numerous case studies complementing the theoretical aspects of the subject, and focusing on genetic diagnostics as well as on prenatal and fertility-related genetic counseling, this book is the first of its kind and includes the latest research on sSMCs.

Human beings normally have a total of 46 chromosomes, with each chromosome present twice, apart from the X and Y chromosomes in males. Some three million people worldwide, however, have 47 chromosomes: they have a small supernumerary marker chromosome (sSMC) in addition to the 46 normal ones. This sSMC can originate from any one of the 24 human chromosomes and can have different shapes. Approximately one third of sSMC carriers show clinical symptoms, while the remaining two thirds manifest no phenotypic effects.

This guide represents the first book ever published on this topic. It presents the latest research results on sSMC and current knowledge about the genotype-phenotype correlation. The focus is on genetic diagnostics as well as on prenatal and fertility-related genetic counseling. A unique feature is that research meets practice: numerous patient reports complement the clinical aspects and depict the experiences of families living with a family member with an sSMC.

Introduction.- Inheritance of sSMC.- Formation of sSMC.- sSMC in genetic diagnostics and counseling.- sSMC known to be correlated with specific syndromes.- Centric sSMC.- Neocentric sSMC by chromosome.- Multiple sSMC.- sSMC additionally to other chromosomal rearrangements.- Complex sSMC.- sSMC and tumor.- Appendix: Patient organizations in connection with sSMC.-Glossary.

Erscheint lt. Verlag 26.1.2014
Zusatzinfo XX, 220 p.
Verlagsort Berlin
Sprache englisch
Maße 155 x 235 mm
Gewicht 370 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Laboratoriumsmedizin
Studium 1. Studienabschnitt (Vorklinik) Histologie / Embryologie
Studium 2. Studienabschnitt (Klinik) Humangenetik
Schlagworte Cat eye syndrome • cytogenetics • Emanuel syndrome • Genetic counseling • Human chromosomes • Isochromosome • Pallister-Killian syndrome • Trisomy • Turner-syndrome
ISBN-10 3-642-43536-X / 364243536X
ISBN-13 978-3-642-43536-2 / 9783642435362
Zustand Neuware
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