Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

Slurred speech, excessive salivation, and hoarseness may be the presenting feature in what percentage of ALS patients? a. \(15 \%\) b. \(25 \%\) c. \(35 \%\) d. \(45 \%\)

Short Answer

Expert verified
Answer Choices: A) 15% B) 25% C) 35% D) 45%

Step by step solution

01

Understand ALS and its symptoms

The first step is to understand what ALS is and familiarize yourself with its symptoms. ALS stands for Amyotrophic Lateral Sclerosis, which is a neurodegenerative disorder affecting both upper and lower motor neurons in the brain and spinal cord. This leads to muscle weakness, resulting in progressive disability and eventually death.
02

Research common symptoms of ALS

Next, find authoritative resources on ALS and its symptoms, such as textbooks, research articles, or reputable websites. From the available resources, identify common symptoms of ALS and their frequency among patients.
03

Analyze the specific symptoms mentioned in the exercise

After getting a general understanding of ALS symptoms, focus on the specific symptoms mentioned in the exercise: slurred speech (dysarthria), excessive salivation (sialorrhea), and hoarseness. Determine the percentage of ALS patients presenting these symptoms.
04

Compare the research findings with the given options

Once you have the percentage of ALS patients presenting slurred speech, excessive salivation, and hoarseness from the relevant sources, compare the findings with the options provided in the exercise: \(15\%\), \(25\%\), \(35\%\), and \(45\%\)
05

Choose the correct answer based on the comparison

Finally, based on the percentage obtained from the research, choose the most accurate option among the given choices in the exercise. This will be the correct answer for the percentage of ALS patients presenting with slurred speech, excessive salivation, and hoarseness.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis (ALS) is a severe neurological condition known for its rapid progression and debilitating symptoms. Primarily affecting the motor neurons - the nerve cells responsible for controlling voluntary muscle movement - ALS results in the gradual loss of muscle function.

Early symptoms of ALS can be subtle, with many patients experiencing muscle weakness or stiffness as initial signs. As the disease progresses, individuals may struggle with tasks such as walking, talking, eating, and breathing. Some also experience cognitive changes, although these are less common.

Understanding the presentation and progression of ALS is crucial, not only for diagnosis and treatment but also for supporting patients and families as they navigate this challenging condition.
Neurodegenerative Disorders
Neurodegenerative disorders encompass a group of diseases characterized by the gradual loss of neurons within the central nervous system. These disorders include conditions like ALS, Parkinson's disease, Alzheimer's disease, and Huntington's disease.

Despite varied symptoms and courses of progression, these disorders typically share common features, such as the loss of specific neurons and the presence of abnormal protein aggregates in the brain. Factors contributing to neurodegeneration include genetics, environmental toxins, and aging.

Research frequently focuses on understanding these diseases' mechanisms to develop more effective treatments. Current therapies primarily aim to manage symptoms and maintain quality of life, reflecting the need for breakthroughs in treatment strategies. With an aging global population, addressing neurodegenerative diseases is increasingly urgent.
Motor Neuron Disease
Motor Neuron Disease (MND) refers to a group of illnesses that affect the motor neurons in the brain and spinal cord. ALS is a form of MND, which is particularly aggressive and has the most significant impact on life expectancy.

Signs of MND include muscle cramps, twitching, and progressive weakness. As with ALS, these symptoms can lead to increasing physical disability. Because motor neurons control the muscles for speaking, swallowing, and breathing, MND can affect these vital functions as well.

Treatment approaches for MND are multidisciplinary, involving medications to slow progression, physical therapy to maintain movement, and assistive technologies to support daily activities. Public awareness and education about these diseases are vital for improving patient outcomes.
Neuroimmune Pharmacology
Neuroimmune Pharmacology is a research field investigating the intersection of the nervous system, the immune system, and pharmacology. This area is gaining traction as scientists recognize the immune system's role in various neurodegenerative disorders, including ALS.

Researchers aim to understand how immune responses contribute to neuron damage and how this knowledge can lead to novel therapies. Potential treatments being explored include immune modulators and anti-inflammatory drugs that target specific immune pathways involved in neurodegeneration.

While this field is relatively new, its insights hold the promise of transformative treatments that could potentially halt or reverse the progression of diseases like ALS, revolutionizing neurodegenerative disease management.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Although human and animal studies support a role for immune responsesin ALSpathogenesis, whichstatement(s) are reasonable explanations for why immunosuppressive therapy has failed in treating ALS? 1\. Immune suppressive therapy is initiated beyond the point when motor neuron recovery and clinical improvement are possible. 2\. Inadequate access to or suppression of immune inflammatory cells in the CNS 3\. Suppression of both cytotoxic and protective immune mechanisms 4\. Immune inflammation does not contribute to ALS disease pathogenesis a. \(1,2,3\) b. 1,3 c. 2,4 d. 4 only e. All of the above

A clinical diagnosis of ALS requires the demonstration of lower motor neuron involvement in which three areas? a. upper extremity limb, eye muscles, and paraspinous muscles b. lower extremity limb, eye muscles, and tongue c. upper extremity limb, tongue, paraspinous muscles d. lower extremity limb, upper extremity, eye muscles

Cognitive dysfunction is not a typical feature of ALS. True/False

Prostaglandins have a dual role in either promoting neuronal survival or apoptotic death. What factors may determine which role predominates in CNS injury or degeneration? 1\. Target cell and tissue environment, degree of cellular response to the inflammatory mediators, and profile of specific prostaglandin(s) 2\. Exposure to prostaglandin and cox-2 inhibitors, target cell and tissue environment, and profile of specific prostaglandins(s) a. both 1 and 2 b. neither 1 or 2 c. 1 d. 2

Association between viral infection and motor neuron disease is based upon cases of motor neuron disease due to retroviral infection (HIV, HTLV-1) and the presence of serum antibodies directed toward endogenous retroviral gene sequences in ALS patients. True/False

See all solutions

Recommended explanations on Biology Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free