The life expectancy of an individual with CF. Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.

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Answer 1

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Chapter 13, Problem 35P

Summary Introduction

To determine: The life expectancy of an individual with CF.

Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.

Summary Introduction

To determine: The usual cause of death in CF.

Introduction: In cystic fibrosis, there are various types of mutations that take place in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This gene has been recognized and related to the proteins that are involved in chloride ion transport in the mucus-cell membrane. This defect of exocrine glands causes abnormal condensed mucus secretion. This mucus secretion is seen in the case of primary cystic fibrosis. Cystic fibrosis is a hereditary disease that is inherited in an autosomal recessive manner.

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Classroom Learning Objectives: Analyze the basic concept of nutrition (MPO 1.1) Discuss factors that affect food choice (MPO 1.2) Define nutrients and classify nutrients according to their work in the body (MPO 1.2) List the functions of water in the body (MPO 1.1) Describe the best practices for assessing a patient’s nutritional needs (MPO 1.2) Identify lab testing that may be completed to assess a patient’s nutritional status (MPO 1.2) Identify select alterations in nutrition with associated manifestations. Describe the multisystem effects of undernutrition (MPO 1.1) Discern when diet modifications may be warranted (MPO 2.3) Apply therapeutic nursing interventions when an alteration in nutritional status is identified. Explain the basic aspects of reading a food label (MPO 1.2) Describe pharmacological treatments of nutritional needs (MPO 1.3)

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Answer 2

Question

Chapter 13, Problem 35P

Summary Introduction

To determine: The life expectancy of an individual with CF.

Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.

Summary Introduction

To determine: The usual cause of death in CF.

Introduction: In cystic fibrosis, there are various types of mutations that take place in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This gene has been recognized and related to the proteins that are involved in chloride ion transport in the mucus-cell membrane. This defect of exocrine glands causes abnormal condensed mucus secretion. This mucus secretion is seen in the case of primary cystic fibrosis. Cystic fibrosis is a hereditary disease that is inherited in an autosomal recessive manner.

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Answer 3

Question

Chapter 13, Problem 35P

Summary Introduction

To determine: The life expectancy of an individual with CF.

Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.

Summary Introduction

To determine: The usual cause of death in CF.

Introduction: In cystic fibrosis, there are various types of mutations that take place in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This gene has been recognized and related to the proteins that are involved in chloride ion transport in the mucus-cell membrane. This defect of exocrine glands causes abnormal condensed mucus secretion. This mucus secretion is seen in the case of primary cystic fibrosis. Cystic fibrosis is a hereditary disease that is inherited in an autosomal recessive manner.

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Answer 4

Question

Chapter 13, Problem 35P

Summary Introduction

To determine: The life expectancy of an individual with CF.

Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.

Summary Introduction

To determine: The usual cause of death in CF.

Introduction: In cystic fibrosis, there are various types of mutations that take place in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This gene has been recognized and related to the proteins that are involved in chloride ion transport in the mucus-cell membrane. This defect of exocrine glands causes abnormal condensed mucus secretion. This mucus secretion is seen in the case of primary cystic fibrosis. Cystic fibrosis is a hereditary disease that is inherited in an autosomal recessive manner.

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Answer 5

Chapter 13, Problem 35P

Summary Introduction

To determine: The life expectancy of an individual with CF.

Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.

Summary Introduction

To determine: The usual cause of death in CF.

Introduction: In cystic fibrosis, there are various types of mutations that take place in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This gene has been recognized and related to the proteins that are involved in chloride ion transport in the mucus-cell membrane. This defect of exocrine glands causes abnormal condensed mucus secretion. This mucus secretion is seen in the case of primary cystic fibrosis. Cystic fibrosis is a hereditary disease that is inherited in an autosomal recessive manner.

Answer 6

Chapter 13, Problem 35P

Summary Introduction

To determine: The life expectancy of an individual with CF.

Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.

Answer 7

Chapter 13, Problem 35P

Summary Introduction

To determine: The life expectancy of an individual with CF.

Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.

Answer 8

Summary Introduction

To determine: The usual cause of death in CF.

Introduction: In cystic fibrosis, there are various types of mutations that take place in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This gene has been recognized and related to the proteins that are involved in chloride ion transport in the mucus-cell membrane. This defect of exocrine glands causes abnormal condensed mucus secretion. This mucus secretion is seen in the case of primary cystic fibrosis. Cystic fibrosis is a hereditary disease that is inherited in an autosomal recessive manner.

Answer 9

Summary Introduction

To determine: The usual cause of death in CF.

Introduction: In cystic fibrosis, there are various types of mutations that take place in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This gene has been recognized and related to the proteins that are involved in chloride ion transport in the mucus-cell membrane. This defect of exocrine glands causes abnormal condensed mucus secretion. This mucus secretion is seen in the case of primary cystic fibrosis. Cystic fibrosis is a hereditary disease that is inherited in an autosomal recessive manner.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 13 - Prob. 1P Ch. 13 - Prob. 2P Ch. 13 - Prob. 3P Ch. 13 - Prob. 4P Ch. 13 - Prob. 5P Ch. 13 - Prob. 6P Ch. 13 - Prob. 7P Ch. 13 - Prob. 8P Ch. 13 - Prob. 9P Ch. 13 - Prob. 10P

The life expectancy of an individual with CF. Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.

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To determine: The life expectancy of an individual with CF.

Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.

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Chapter 13 Solutions

The life expectancy of an individual with CF. Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.

Concept explainers

Videos

To determine: The life expectancy of an individual with CF. Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.

Want to see the full answer?

Chapter 13 Solutions

To determine: The life expectancy of an individual with CF.

Introduction: Cystic fibrosis (CF) is an inherited genetic disorder in the case of children. It is also known as mucoviscidosis.