Treatment of hypotonia

Hypotonia or weakness of muscles and lack of muscle tone is a symptom of an underlying condition rather than a disease entity in itself.

Therapy involves treating the symptoms as well as the underlying conditions.

Therapy team

The therapy team is usually multidisciplinary. The team involves:

  • a paediatrician
  • neurologist
  • orthopaedic surgeon
  • chest specialist
  • heart specialist
  • physiotherapist
  • physical and occupational therapist
  • speech and language therapist
  • sometimes genetic counsellors

Types of therapy for hypotonia

There are several types of therapy for hypotonia, these include physiotherapy, occupational therapy and so forth. (1-4)

Physiotherapy

Regular physiotherapy is important to improve muscle tone and prevent contractures.

Physiotherapy aims to improve posture, and co-ordination and strengthen the muscles around the joints of the limbs to provide more stability and support.

Regular exercises are prescribed for this purpose.

Occupational therapy

Occupational therapy helps patients in the activities of daily living.

For example, fine finger skills are focussed upon to improve feeding and dressing etc.

Speech and language therapy

Speech and language therapy is recommended for patients who have speech and swallowing problems due to hypotonia.

This therapy helps develop better control of the jaw and mouth muscles.

Assisted breathing

Patients with hypotonia often suffer from difficulty in breathing at night due to further loss of muscle tone.

These patients need assisted artificial breathing and ventilation through machines.

They are also at risk of repeated respiratory infections that need to be treated. Annual flu vaccination is necessary.

Orthopaedic review

Orthopaedic review is important annually to check for spinal deformities, hip dislocation and joint weakness and slipping (subluxation).

Some patients may need braces and surgical procedures to improve movement and support of the limbs.

Feeding interventions

In babies and children with severe hypotonia and difficulty in feeding, interventions like tube feeding may be needed.

Ideal weight maintenance and adequate nutrition is important part of management.

Specific medication

Babies with myasthenia gravis need specific medication. These are drugs like Neostigmine, Physostigmine etc.

The treatment may often last a life time.

In myasthenia gravis the body’s immune system attacks certain receptors at the neuromuscular junction. Sometimes drugs that suppress the immunity like corticosteroids may be added to regular myasthenia gravis therapy to relieve symptoms of muscle weakness.

Antibiotics

Hypotonia may be caused due to an infection, meningitis or encephalitis.

If antibiotics are administered to fight these infections, symptoms may be reduced.

Therapy for genetic disorders causing hypotonia

Genetic disorders like Down’s syndrome, Prader Willi syndrome, Marfan’s syndrome, Ehler-Danlos syndrome etc. do not always have specific therapy.

These conditions with hypotonia may be treated symptomatically with physical and occupational therapy.

Genetic counselling may be offered to parents regarding future pregnancies.

Therapies are not always needed

Premature babies who are born with hypotonia often recover by themselves as they grow. They may need vigilance against infections, sepsis and feeding difficulties.

Babies with no specific cause of hypotonia called Benign congenital hypotonia often need no therapy apart from physical and occupational therapy.

Further Reading

Last Updated: Jun 11, 2023

Dr. Ananya Mandal

Written by

Dr. Ananya Mandal

Dr. Ananya Mandal is a doctor by profession, lecturer by vocation and a medical writer by passion. She specialized in Clinical Pharmacology after her bachelor's (MBBS). For her, health communication is not just writing complicated reviews for professionals but making medical knowledge understandable and available to the general public as well.

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Comments

  1. s. p. s. p. India says:

    My grandson is treated for significant high levels of glycine levels of CSF/plasma mild levels of glycine as per aster CMI hospital banglore neurologists. Plasma/csf ratio levels of elevated glycine is.0.39 . Elevated levels of glycine plasma 554umol/L&csf elevated levels of glycine 217umol/Lsodiumbenzoate/dextromethorphone dosage 500mg/day&25mgdexomethorphone administered two time per day for 3months as per neurologists of aster CMI. Is the kid now one year having no history of genetic problem as per kg hospital gynecology chief &neurologists of kg hospital Coimbatore at time of birth. Is child can become normal? Pl. Reply.

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