| Hypotonia - Floppy Muscle Syndrome |
| Classification and external resources |
| ICD-10 |
P94.2 |
| ICD-9 |
358,781.3 |
| DiseasesDB |
21417 |
| MedlinePlus |
003298 |
| MeSH |
D009123 |
Hypotonia is a state of low muscle tone[1] (the amount of tension or resistance to stretch 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, occupational therapy for remediation, and/or music therapy.
Hypotonia is thought to be associated with the disruption of afferent input from stretch receptors and/or lack of the cerebellum’s facilitatory efferent influence on the fusimotor system, the system that innervates intrafusal muscle fibers thereby controlling muscle spindle sensitivity.[2] On examination a diminished resistance to passive movement will be noted and muscles may feel abnormally soft and limp on palpation.[2] Diminished deep tendon reflexes also may be noted.
Hypotonia is a condition that can be helped with early intervention.[citation needed]
Contents
- 1 Etiology of hypotonia
- 2 Signs and objective manifestations
- 2.1 Floppy baby syndrome
- 2.2 Developmental delay
- 2.3 Muscle tone vs. muscle strength
- 3 Diagnosis
- 4 Prognosis and treatment
- 5 See also
- 6 References
- 7 Further reading
- 8 External links
Etiology of hypotonia
Some conditions known to cause hypotonia include:
Congenital - i.e. disease a person is born with (including genetic disorders presenting within 6 months)
- Genetic disorders are the most common cause
- 22q13 deletion syndrome aka Phelan-McDermid Syndrome
- 3-Methylcrotonyl-CoA carboxylase deficiency [3]
- Achondroplasia
- Aicardi syndrome
- Autism Spectrum Disorders[4]
- Canavan disease
- Centronuclear myopathy (including myotubular myopathy)
- Central core disease
- Cohen Syndrome
- Costello Syndrome
- Dejerine Sottas syndrome (HMSN Type III)
- Down syndrome aka trisomy 21 — most common
- Ehlers-Danlos Syndrome
- Familial dysautonomia (Riley-Day syndrome)
- FG syndrome
- Fragile X syndrome
- Griscelli syndrome Type 1 (Elejalde Syndrome)
- Disorder Growth Hormone Disorder Pituitary Dwarfism
- Holocarboxylase synthetase deficiency / Multiple carboxylase deficiency[5]
- Krabbe disease
- Leigh's disease
- Marfan's syndrome
- Menkes syndrome
- Methylmalonic acidemia
- Myotonic dystrophy
- Niemann-Pick disease
- Nonketotic hyperglycinemia (NKH) or Glycine encephalopathy (GCE)
- Noonan Syndrome
- Neurofibromatosis
- Patau syndrome aka trisomy 13
- Prader-Willi syndrome
- Rett syndrome
- Septo-optic dysplasia (de Morsier syndrome)
- Spinal Muscular Atrophy (SMA)
- Succinic semialdehyde dehydrogenase deficiency (SSADH)
- Tay-Sachs disease
- Williams syndrome
- Zellweger syndrome aka cerebrohepatorenal syndrome
- Developmental disability
- Cerebellar ataxia (congenital)
- Sensory processing disorder
- Developmental coordination disorder
- 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
- Toxins
- Infantile acrodynia (childhood mercury poisoning)
- Autoimmunity disorders
- Myasthenia gravis - most common
- Abnormal vaccine reaction
- Celiac Disease [6]
- 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 and cerebral palsy
- Hypothyroidism
- Sandifer syndrome
- neonatal Benzodiazepine withdrawal syndrome in children born to mothers treated in late pregnancy with benzodiazepine medications[7]
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. 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 people with hypotonia 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".[citation needed] 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 sometimes 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 intellectual disability, that may be associated with the cause of hypotonia. Additionally, lower muscle tone can be caused by Mikhail-Mikhail syndrome, which is characterized by muscular atrophy and cerebellar ataxia which is due to abnormalities in the ATXN1 gene.
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, quickly straighten the flexed elbow of an unsuspecting child with normal tone, will cause their biceps to contract in response (automatic protection against possible injury). When the perceived danger has passed, (which the brain figures out once the stimulus is removed), the muscle 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 realizing their full potential of maintaining a muscle contraction over time. "
Diagnosis
The approach to diagnosing the etiology of hypotonia (as with all syndromes in neurology) is first localization. The physician must first determine if the hypotonia is due to muscle, nmj, nerve, or central etiology. This will narrow the etiological possibilities. If the cause of the hypotonia is found to lie in the brain, then it can be classified as a cerebral palsy. If the cause is localized to the muscles, it can be classified as a muscular dystrophy. If the cause is thought to be in the nerves, it is call hypotonia due to polyneuropathy. Many cases cannot be definitively diagnosed. "[8]
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.
Terminology
The term hypotonia comes from the Ancient Greek ὑπο- (hypo-), "under" and τόνος (tónos), from τείνω (teinō), "to stretch". Other terms for the condition include:
- 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 lifelong. 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).
The National Institute of Neurological Disorders and Stroke states that physical therapy can improve motor control and overall body strength in individuals with hypotonia. This is crucial to maintaining both static and dynamic postural stability, which is important since postural instability is a common problem in people with hypotonia.[2] A physiotherapist can develop patient specific training programs to optimize postural control, in order to increase balance and safety.[2] To protect against postural asymmetries the use of supportive and protective devices may be necessary.[2] Physical therapists might use neuromuscular/sensory stimulation techniques such as quick stretch, resistance, joint approximation, and tapping to increase tone by facilitating or enhancing muscle contraction in patients with hypotonia.[2] For patients who demonstrate muscle weakness in addition to hypotonia strengthening exercises that do not overload the muscles are indicated.[2] Electrical Muscle Stimulation, also known as Neuromuscular Electrical Stimulation (NMES) can also be used to “activate hypotonic muscles, improve strength, and generate movement in paralyzed limbs while preventing disuse atrophy (p.498).”[2] When using NMES it is important to have the patient focus on attempting to contract the muscle(s) being stimulated. Without such concentration on movement attempts, carryover to volitional movement is not feasible.[2] NMES should ideally be combined with functional training activities to improve outcomes.
Occupational therapy can assist the patient with increasing independence with daily tasks through improvement of motor skills, strength, and functional endurance. Speech-language therapy can help with any breathing, speech, and/or swallowing difficulties the patient may be having. Therapy for infants and young children may also include sensory stimulation programs." A physical therapist may recommend an ankle/foot orthosis to help the patient compensate for weak lower leg muscles. Toddlers and children with speech difficulties may benefit greatly by using sign language.
See also
References
- ^ "Hypotonia". MedlinePlus Medical Encyclopedia.
- ^ a b c d e f g h i O'Sullivan S. B. (2007). Strategies to Improve Motor Function. In S. B. O’Sullivan, & T. J. Schmitz (Eds.), Physical Rehabilitation (5th Ed.) Philadelphia: F.A. Davis Company.
- ^ "3-methylcrotonyl-CoA carboxylase deficiency (3-MCC deficiency)". Genetics Home Reference. Retrieved 28 November 2013.
- ^ Xue Ming, et al. Prevalence of motor impairment in autism spectrum disorders. Brain and Development. Volume 29, Issue 9, October 2007, Pages 565–570.
- ^ "Holocarboxylase Synthetase Deficiency / Multiple Carboxylase Deficiency -". HLCS Gene Sequencing. GeneDx. Retrieved 28 November 2013.
- ^ Zelnik N, Pacht A, Obeid R, Lerner A (June 2004). "Range of neurologic disorders in patients with celiac disease". Pediatrics 113 (6): 1672–6. doi:10.1542/peds.113.6.1672. PMID 15173490.
- ^ McElhatton PR. (Nov–December 1994). "The effects of benzodiazepine use during pregnancy and lactation". Reprod Toxicol. 8 (6): 461–75. doi:10.1016/0890-6238(94)90029-9. PMID 7881198.
- ^ "The Benign Congenital Hypotonia Site". Retrieved 2007-06-07.
Further reading
- 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 17 (4): 275–82. doi:10.1097/01.pep.0000186506.48500.7c. PMID 16357683.
External links
- Early recognition and intervention is the key to recovery for Benign Congenital Hypotonia - Shannon Munro Cohen, RNC, BSN, and Teresa Whitt, Ph.D.
- hypotonia at NINDS
- Encyclopedia of Children's Health
- Hypotonia - Medline Plus
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Diseases of myoneural junction and muscle / neuromuscular disease (G70–G73, 358–359)
|
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Neuromuscular-
junction disease |
- autoimmune
- Myasthenia gravis
- Lambert–Eaton myasthenic syndrome
|
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Myopathy/
congenital myopathy |
Muscular dystrophy
(DAPC) |
| AD |
- Limb-girdle muscular dystrophy 1
- Oculopharyngeal
- Facioscapulohumeral
- Myotonic
- Distal (most)
|
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| AR |
- Limb-girdle muscular dystrophy 2
- Congenital
- Fukuyama
- Ullrich
- Walker–Warburg
|
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| XR |
- dystrophin
- Emery–Dreifuss
|
|
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| Other structural |
- collagen disease
- PTP disease
- adaptor protein disease
- BIN1-linked centronuclear myopathy
- cytoskeleton disease
- Nemaline myopathy
- Zaspopathy
|
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| Channelopathy |
| Myotonia |
- Myotonia congenita
- Thomsen disease
- Neuromyotonia/Isaacs syndrome
- Paramyotonia congenita
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| Periodic paralysis |
|
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| Other |
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| Mitochondrial myopathy |
|
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| Other |
|
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|
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anat (h/n, u, t/d, a/p, l)/phys/devp/hist
|
noco (m, s, c)/cong (d)/tumr, sysi/epon, injr
|
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|
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Certain conditions originating in the perinatal period / fetal disease (P, 760–779)
|
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Maternal factors and
complications of pregnancy,
labour and delivery |
| placenta: |
- Placenta praevia
- Placental insufficiency
- Twin-to-twin transfusion syndrome
|
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| chorion/amnion: |
|
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| umbilical cord: |
- Umbilical cord prolapse
- Nuchal cord
- Single umbilical artery
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Length of gestation
and fetal growth |
- Small for gestational age/Large for gestational age
- Preterm birth/Postmature birth
- Intrauterine growth restriction
|
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| Birth trauma |
- scalp
- Cephalhematoma
- Chignon
- Caput succedaneum
- Subgaleal hemorrhage
- Brachial plexus lesion
- Erb's palsy
- Klumpke paralysis
|
|
| By system |
| Respiratory |
- Intrauterine hypoxia
- Infant respiratory distress syndrome
- Transient tachypnea of the newborn
- Meconium aspiration syndrome
- pleural disease
- Pneumothorax
- Pneumomediastinum
- Wilson–Mikity syndrome
- Bronchopulmonary dysplasia
|
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| Cardiovascular |
- Pneumopericardium
- Persistent fetal circulation
|
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Haemorrhagic and
hematologic disease |
- Vitamin K deficiency
- Haemorrhagic disease of the newborn
- HDN
- ABO
- Anti-Kell
- Rh c
- Rh D
- Rh E
- Hydrops fetalis
- Hyperbilirubinemia
- Kernicterus
- Neonatal jaundice
- Velamentous cord insertion
- Intraventricular hemorrhage
- Germinal matrix hemorrhage
- Anemia of prematurity
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| Digestive |
- Ileus
- Necrotizing enterocolitis
- Meconium peritonitis
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Integument and
thermoregulation |
- Erythema toxicum
- Sclerema neonatorum
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| Nervous system |
- Periventricular leukomalacia
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| Musculoskeletal |
- Gray baby syndrome
- muscle tone
- Congenital hypertonia
- Congenital hypotonia
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| Infectious |
- Vertically transmitted infection
- Congenital rubella syndrome
- Neonatal herpes simplex
- Omphalitis
- Neonatal sepsis
- Group B streptococcal infection
- Neonatal conjunctivitis
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| Other |
- Perinatal mortality
- Stillbirth
- Infant mortality
- Neonatal withdrawal
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