HUMAN BIOLOGY (LOOSELEAF)-W/CONNECT
HUMAN BIOLOGY (LOOSELEAF)-W/CONNECT
16th Edition
ISBN: 9781260692174
Author: Mader
Publisher: MCG
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Chapter 13.4, Problem 3CYP
Summary Introduction

To analyze:

The symptoms of muscular dystrophy.

Introduction:

A group of muscle diseases where increasing weakening and breakdown of skeletal muscles takes place is known as muscular dystrophy.

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*Example 2: Tracing the path of an autosomal dominant trait Trait: Neurofibromatosis Forms of the trait: The dominant form is neurofibromatosis, caused by the production of an abnormal form of the protein neurofibromin. Affected individuals show spots of abnormal skin pigmentation and non-cancerous tumors that can interfere with the nervous system and cause blindness. Some tumors can convert to a cancerous form. i The recessive form is a normal protein - in other words, no neurofibromatosis.moovi A typical pedigree for a family that carries neurofibromatosis is shown below. Note that carriers are not indicated with half-colored shapes in this chart. Use the letter "N" to indicate the dominant neurofibromatosis allele, and the letter "n" for the normal allele. Nn nn nn 2 nn Nn A 3 N-
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