Hypotonia

Hypotonia-Floppy Muscle Syndrome-Chris Lord
Classification and external resources
ICD-10	P94.2
ICD-9	358
DiseasesDB	21417
MeSH	D009123

Hypotonia is a state of low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle strength. Hypotonia is not a specific medical disorder, but a potential manifestation of many different diseases and disorders that affect motor nerve control by the brain or muscle strength. Recognizing hypotonia, even in early infancy, is usually relatively straightforward, but diagnosing the underlying cause can be difficult and often unsuccessful. The long-term effects of hypotonia on a child's development and later life depend primarily on the severity of the muscle weakness and the nature of the cause. Some disorders have a specific treatment but the principal treatment for most hypotonia of idiopathic or neurologic cause is physical therapy and/or occupational therapy to help the person compensate for the neuromuscular disability.

Hypotonia is a condition that can be helped with early intervention.

Etiology of hypotonia

Some conditions known to cause hypotonia include:

Congenital

Congenital - i.e. disease you are born with (including genetic disorders presenting within 6 months)

• Genetic disorders are the most common cause
  • Down syndrome - most common
  • 3-Methylcrotonyl-CoA carboxylase deficiency
  • Achondroplasia
  • Aicardi syndrome
  • Canavan disease
  • Centronuclear myopathy (including myotubular myopathy)
  • Central core disease
  • Dejerine Sottas syndrome (HMSN Type III)
  • Familial dysautonomia (Riley-Day syndrome)
  • Griscelli syndrome Type 1 (Elejalde Syndrome)
  • Growth Hormone Disorder Pituitary Dwarfism
  • Infantile spinal muscular atrophy such as Werdnig-Hoffman disease
  • Krabbe disease
  • Leigh's disease
  • Marfan's syndrome
  • Menkes syndrome
  • Methylmalonic acidemia
  • Myotonic dystrophy
  • Niemann-Pick disease
  • Nonketotic hyperglycinemia (NKH) or Glycine encephalopathy (GCE)
  • Prader-Willi syndrome
  • Rett syndrome
  • Septo-optic dysplasia (de Morsier syndrome)
  • Spinal Muscular Atrophy (SMA)
  • Tay-Sachs disease
  • Trisomy 13
  • 22q13 deletion syndrome
  • FG syndrome

• Developmental disability
  • Cerebellar ataxia (congenital)
  • Sensory integration dysfunction
  • Developmental dyspraxia
  • Hypothyroidism (congenital)
  • Hypotonic cerebral palsy
  • Teratogenesis from in utero exposure to Benzodiazepines

Acquired

Acquired - i.e. onset occurs after birth

• Genetic
  • Muscular dystrophy (including Myotonic dystrophy) - most common
  • Metachromatic leukodystrophy
  • Rett Syndrome
  • Spinal Muscular Atrophy

• Infections
  • Encephalitis
  • Guillain-Barré syndrome
  • Infant botulism
  • Meningitis
  • Poliomyelitis
  • Sepsis

• Autoimmunity disorders
  • Myasthenia gravis - most common
  • Abnormal vaccine reaction
  • Celiac Disease

• Metabolic disorder
  • Hypervitaminosis
  • Kernicterus
  • Rickets

• Neurological
  • Traumatic brain injury, such as the damage that is caused by Shaken Baby Syndrome
  • Lower motor neuron lesions
  • Upper motor neuron lesions

• Miscellaneous
  • Central nervous system dysfunction, including Cerebellar lesions
  • Hypothyroidism

Signs and objective manifestations

Hypotonic patients may display a variety of objective manifestations that indicate decreased muscle tone. Motor skills delay is often observed, along with hypermobile or hyperflexible joints, drooling and speech difficulties, poor reflexes, decreased strength, decreased activity tolerance, rounded shoulder posture, with leaning onto supports, and poor attention and motivation. The extent and occurrence of specific objective manifestations depends upon the age of the patient, the severity of the hypotonia, the specific muscles affected, and sometimes the underlying cause. For instance, some hypotonics may experience constipation, while others have no bowel problems.

Floppy baby syndrome

The term "floppy infant syndrome" is used to describe abnormal limpness when an infant is prone.

Infants who suffer from hypotonia are often described as feeling and appearing as though they are "rag dolls," a "sack of jello" or a "pillow full of puddin'," easily slipping through one's hands. This image demonstrates the floppiness of a hypotonic infant. They are unable to maintain flexed ligaments, and are able to extend them beyond normal lengths. Often, the movement of the head is uncontrollable, not in the sense of spasmatic movement, but chronic ataxia. Hypotonic infants often have difficulty feeding, as their mouth muscles cannot maintain a proper suck-swallow pattern, or a good breastfeeding latch.

Developmental delay

Children with normal muscle tone are expected to achieve certain physical abilities within an average timeframe after birth. Most low-tone infants have delayed developmental milestones, but the length of delay can vary widely. Motor skills are particularly susceptible to the low-tone disability. They can be divided into two areas, gross motor skills, and fine motor skills, both of which are affected. Hypotonic infants are late in lifting their heads while lying on their stomachs, rolling over, lifting themselves into a sitting position, remaining seated without falling over, balancing, crawling, and walking. Fine motor skills delays occur in grasping a toy or finger, transferring a small object from hand to hand, pointing out objects, following movement with the eyes, and self feeding.

Speech difficulties can result from hypotonia. Low-tone children learn to speak later than their peers, even if they appear to understand a large vocabulary, or can obey simple commands. Difficulties with muscles in the mouth and jaw can inhibit proper pronunciation, and discourage experimentation with word combination and sentence-forming. Since the hypotonic condition is actually an objective manifestation of some underlying disorder, it can be difficult to determine whether speech delays are a result of poor muscle tone, or some other neurological condition, such as mental retardation, that may be associated with the cause of hypotonia.

Muscle tone vs. muscle strength

The low muscle tone associated with hypotonia must not be confused with low muscle strength or the definition commonly used in body building. Neurologic muscle tone is a manifestation of periodic action potentials from motor neurons. As it is an intrinsic property of the nervous system, it cannot be changed through voluntary control, exercise, or diet.

"True muscle tone is the inherent ability of the muscle to respond to a stretch. For example, if you quickly straighten the flexed elbow of an unsuspecting child with normal tone, the biceps will quickly contract in response (automatic protection against possible injury). When the perceived danger has passed, which the brain figures out really quickly once the stimulus is removed, the muscle then relaxes, and returns to its normal resting state.

"...The child with low tone has muscles that are slow to initiate a muscle contraction, contract very slowly in response to a stimulus, and cannot maintain a contraction for as long as his 'normal' peers. Because these low-toned muscles do not fully contract before they again relax (muscle accommodates to the stimulus and so shuts down again), they remain loose and very stretchy, never realising their full potential of maintaining a muscle contraction over time. "

Diagnosis

"A diagnosis of hypotonia is sometimes considered a form of muscular dystrophy or cerebral palsy, depending on the symptoms and the doctor. If the cause of the hypotonia is thought to lie in the brain, then it might be classified as a cerebral palsy. If the cause seems to be in the muscles, it might be classified as a muscular dystrophy, even though most forms of hypotonia are not seriously dystrophic. If the cause is thought to be in the nerves, it could be classified as either or neither. In any case, hypotonia is rarely an actual muscular dystrophy or cerebral palsy, and is often not classified as either one, or anything at all for that matter."

Diagnosing a patient includes obtaining family medical history and a physical examination, and may include such additional tests as computerized tomography (CT) scans, magnetic resonance imaging (MRI) scans, electroencephalogram (EEG), blood tests, genetic testing (such as chromosome karyotyping and tests for specific gene abnormalities), spinal taps, electromyography muscle tests, or muscle and nerve biopsy.

Mild or benign hypotonia is often diagnosed by physical and occupational therapists through a series of exercises designed to assess developmental progress, or observation of physical interactions. Since a hypotonic child has difficulty deciphering his spatial location, he may have some recognizable coping mechanisms, such as locking the knees while attempting to walk. A common sign of low-tone infants is a tendency to observe the physical activity of those around them for a long time before attempting to imitate, due to frustration over early failures. Developmental delay can indicate hypotonia.

Other names for hypotonia

• Low Muscle Tone
• Benign Congenital Hypotonia
• Congenital Hypotonia
• Congenital Muscle Hypotonia
• Congenital Muscle Weakness
• Amyotonia Congenita
• Floppy Baby Syndrome
• Infantile Hypotonia

Prognosis and treatment

There is currently no known treatment or cure for most (or perhaps all) causes of hypotonia, and objective manifestations can be life long. The outcome in any particular case of hypotonia depends largely on the nature of the underlying disease. In some cases, muscle tone improves over time, or the patient may learn or devise coping mechanisms that enable them to overcome the most disabling aspects of the disorder. However, hypotonia caused by cerebellar dysfunction or motor neuron diseases can be progressive and life-threatening.

Along with normal pediatric care, specialists who may be involved in the care of a child with hypotonia include developmental pediatricians (specialize in child development), neurologists, neonatologists (specialize in the care of newborns), geneticists, occupational therapists, physical therapists, speech therapists, orthopedists, pathologists (conduct and interpret biochemical tests and tissue analysis), and specialized nursing care.

If the underlying cause is known, treatment is tailored to the specific disease, followed by symptomatic and supportive therapy for the hypotonia. In very severe cases, treatment may be primarily supportive, such as mechanical assistance with basic life functions like breathing and feeding, physical therapy to prevent muscle atrophy and maintain joint mobility, and measures to try to prevent opportunistic infections such as pneumonia. Treatments to improve neurological status might involve such things as medication for a seizure disorder, medicines or supplements to stabilize a metabolic disorder, or surgery to help relieve the pressure from hydrocephalus (increased fluid in the brain).

For most hypotonics, the National Institute of Health recommends "physical therapy [to] improve motor control and overall body strength. Occupational therapy to assist with fine motor skill development and hand control, and speech-language therapy can help breathing, speech, and swallowing difficulties. Therapy for infants and young children may also include sensory stimulation programs." Ankle/foot orthoses are sometimes used for weak ankle muscles. Toddlers and children with speech difficulties may benefit greatly by using sign language.

See also

• Hypertonia

External links

• Exercises and Stimulation Therapy for Hypotonia from Early Parent Intervention Project (ARC Texas)
• Early recognition and intervention is the key to recovery for Benign Congenital Hypotonia Shannon Munro Cohen, RNC, BSN, and Teresa Whitt, Ph.D.
• Martin K, Inman J, Kirschner A, Deming K, Gumbel R, Voelker L (2005). "Characteristics of hypotonia in children: a consensus opinion of pediatric occupational and physical therapists". Pediatric physical therapy : the official publication of the Section on Pediatrics of the American Physical Therapy Association. 17 (4): 275–82. PMID 16357683. CS1 maint: Multiple names: authors list (link)
• Overview at National Organization of Rare Disorders
• hypotonia at NINDS
• Encyclopedia of Children's Health

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