What causes poor muscle tone? 10 possible conditions

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Hypotonia

Hypotonia, or poor muscle tone, is usually detected at birth or during infancy. If your infant has hypotonia, he or she may appear limp at birth and not be able to keep his or her knees and elbows slightly bent. Your child may continue to struggle with feeding and motor skills.

Many different diseases and disorders cause the symptoms of hypotonia. It is easily recognizable because it affects muscle strength, motor nerves, and the brain. However, diagnosing the disease or disorder that is causing the problem can be challenging.

Hypotonia is sometimes called floppy muscle syndrome.

Signs of Hypotonia

Depending on the underlying cause, hypotonia can appear at any age. Signs of hypotonia in infants and children are:

  • poor or no head control
  • delay in gross motor skills development such as crawling
  • delay in fine motor skills development such as grasping a crayon

Signs of hypotonia at any age are:

  • decrease in muscle tone
  • decrease in strength
  • poor reflexes
  • hyperflexibility
  • speech difficulties
  • decrease in activity endurance
  • weakened posture

Causes of Hypotonia

Hypotonia can be triggered by a problem with the nervous system or muscular system. Sometimes it is the result of injury, illness, or an inherited disorder. Some causes may not be identified.

Some children are born with hypotonia that is not related to a separate condition. This is called benign congenital hypotonia. Physical, occupational, and speech therapy can help your child gain muscle tone and stay on track with development. Some children with benign congenital hypotonia have minor developmental delays or learning disabilities that continue through childhood.

Hypotonia can be caused by underlying conditions that affect the brain, central nervous system, or muscles. These include:

  • cerebral palsy
  • brain damage (often due to lack of oxygen at birth)
  • muscular dystrophy

In many cases, these chronic conditions require lifelong care and treatment.

Hypotonia may also be caused by genetic conditions. Some of these conditions include:

  • Down syndrome
  • Prader-Willi syndrome
  • Tay-Sachs disease
  • Trisomy 13

Children with Down syndrome and Prader-Willi syndrome often benefit from therapy. Children with Tay-Sachs disease and Trisomy 13 typically have shortened lives.

Rarely, hypotonia is caused by botulism infections or contact with poisons or toxins. However, it often goes away after you recover.

When to See a Doctor

Hypotonia may be diagnosed at birth. You may not notice your child’s condition until he or she is older. An indicator is that your child is not meeting developmental milestones. Schedule regular appointments for your child with a doctor and mention concerns you have about your child’s progress.

Your doctor will assess your child’s development and run tests if he or she has concerns. Tests may include blood tests, and MRI and CT scan imaging.

If you notice sudden signs of the condition in a person of any age, seek emergency medical care as soon as possible.

Treating Hypotonia

Treatment varies depending upon how your child is affected. Your child’s general health and ability to participate in therapies will help shape a treatment plan. Some children work frequently with physical therapists. Depending upon your child’s abilities, he or she may work toward specific goals such as sitting upright, walking, or taking part in sports. In some cases, your child may need help with his or her coordination and other fine motor skills.

Children with severe conditions may need wheelchairs for mobility. Hypotonia can cause complications such as frequent joint dislocations and a need for casts or braces to correct and prevent injuries.

What Is the Long-Term Outlook for Patients with Hypotonia?

The long-term outlook depends upon the following:

  • underlying cause
  • age
  • severity
  • muscles affected

Having hypotonia can be challenging. It is often a lifelong condition, and you will need to learn coping mechanisms and may need therapy. However, it is not life threatening, except in the cases of motor neuron or cerebellar dysfunction.

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See a list of possible causes in order from the most common to the least.

1

Muscular Dystrophies

Muscular dystrophies are a group of diseases that cause damage and weakness to muscles over time. This damage and weakness is caused by the lack of a protein called dystrophin, which is necessary for normal muscl...

Read more »

2

Down Syndrome

Down syndrome is a genetic abnormality that occurs due to an extra copy of chromosome 21. It causes lifelong developmental delays that can range from moderate to severe. It cannot be cured but can be managed wit...

Read more »

3

Cerebral Palsy

Cerebral palsy is a disorder of muscle movement and coordination caused by an injury to a child's brain that occurs before birth or during infancy. It affects the part of the brain that controls body movement. Othe...

Read more »

4

Metachromatic Leukodystrophy

Enzymes are proteins that help break down (metabolize) substances in the body. If certain enzymes are not present, the body will be unable to metabolize a substance. If the substance remains in the body, it may buil...

Read more »

5

Achondroplasia

Achondroplasia is a bone growth disorder that causes disproportionate dwarfism. Dwarfism is defined as a condition of short stature as an adult. People with achondroplasia are short in stature with a normal sized tors...

Read more »

6

The Truth Behind Clumsy Child Syndrome: Developmental Coordination Disorder

Children normally develop the ability to sit up, stand, walk, and talk at predictable ages. When they are late in achieving these milestones, it may be due to a developmental problem. Developmental Coordination Disorde...

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7

Hartnup Disease

Hartnup disease, also referred to as Hartnup disorder, is a hereditary metabolic disorder that makes it difficult for your body to absorb certain amino acids from the intestine and to reabsorb these amino acids from th...

Read more »

8

Tay-Sachs Disease

Tay-Sachs is a disease of the central nervous system; it is a neurodegenerative disorder. Tay-Sachs most commonly affects infants. In infants, it is a progressive disease that is unfortunately always fatal. Rarely...

Read more »

9

Isopropyl Alcohol Poisoning

This condition is considered a medical emergency. Urgent care may be required.

Isopropyl alcohol (IPA) poisoning occurs when the liver is no longer able to manage the amount of IPA in the body. Ingestion may be accidental or deliberate. IPA is inexpensive and causes rapid intoxication. It can b...

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10

Aftershave Poisoning

This condition is considered a medical emergency. Urgent care may be required.

Most aftershaves contain the poisonous ingredients. If swallowed, it can produce harmful effects. Symptoms include muscle cramping, nausea, abdominal pain, headache, and dizziness.

Read more »

This feature is for informational purposes only and should not be used to diagnose.
Please consult a healthcare professional if you have health concerns.
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