ex2012: Muscular Dystrophy

ex2012R Documentation

Muscular Dystrophy

Description

Duchenne Muscular Dystrophy (DMD) is a genetically transmitted disease, passed from a mother to her children. Boys with the disease usually die at a young age; but affected girls usually do not suffer symptoms, may unknowingly carry the disease and may pass it to their offspring. It is believed that about 1 in 3,300 women are DMD carriers. A woman might suspect she is a carrier when a related male child develops the disease. Doctors must rely on some kind of test to detect the presence of the disease. This data frame contains data on two enzymes in the blood, creatine kinase (CK) and hemopexin (H) for 38 known DMD carriers and 82 women who are not carriers. It is desired to use these data to obtain an equation for indicating whether a women is a likely carrier.

Usage

ex2012

Format

A data frame with 120 observations on the following 3 variables.

Group

Indicator whether the woman has DMD ("Case") or not ("Control")

CK

Creatine kinase reading

H

Hemopexin reading

Source

Ramsey, F.L. and Schafer, D.W. (2013). The Statistical Sleuth: A Course in Methods of Data Analysis (3rd ed), Cengage Learning.

References

Andrews, D.F. and Herzberg, A.M. (1985). Data: A Collection of Problems From Many Fields For The Student And Research Worker, Springer-Verlag, New York.

Examples

str(ex2012)

Sleuth3 documentation built on Jan. 25, 2024, 3:01 p.m.