Hypotonia

From WikiMD's Wellness Encyclopedia

(Redirected from Floppy infant syndrome)


Hypotonia, often referred to as floppy baby syndrome, is characterized by diminished muscle tone, which is the inherent resistance of muscles to passive stretching. It is crucial to distinguish between muscle tone and muscle strength, as the latter pertains to the capability of muscles to exert force actively. Though hypotonia manifests as a symptom, it is not an isolated medical disorder. Instead, it can signify various underlying diseases or conditions affecting either the motor nerve control from the brain or the muscle strength itself.

1 Signs and symptoms[edit | edit source]

1.1 Floppy baby syndrome[edit | edit source]

Infants with hypotonia may appear limp at birth, resembling a "rag doll". They may rest with their elbows and knees loosely extended, as opposed to the typical flexed position. The baby might also display difficulties with feeding, due to the associated muscle weaknesses.

1.2 Developmental delay[edit | edit source]

Hypotonia may hinder an infant's motor development milestones such as holding the head up, sitting without support, and walking. The delay is due to the diminished muscle strength associated with hypotonia.

1.3 Muscle tone vs. muscle strength[edit | edit source]

Muscle tone refers to the tension present in a muscle when it is passively stretched. In contrast, muscle strength refers to the active force a muscle produces when it contracts. Hypotonia is identified by a lack of resistance to passive stretching, whereas muscle weakness is recognized by impaired active movement.

2 Cause[edit | edit source]

Hypotonia may arise from various underlying causes, either from the central nervous system or the peripheral structures, including the spinal cord, peripheral nerves, and skeletal muscles.

Some conditions known to cause hypotonia include:

Congenital – i.e. disease a person is born with (including genetic disorders presenting within 6 months)

Acquired[edit | edit source]

Acquired – i.e. onset occurs after birth

3 Diagnosis[edit | edit source]

Early detection of hypotonia is generally straightforward, especially in infancy. However, pinpointing the root cause can be intricate and sometimes remains undetermined.

3.1 Terminology[edit | edit source]

  • Central Hypotonia: Originates from issues within the central nervous system.
  • Peripheral Hypotonia: Associated with complications within the spinal cord, peripheral nerves, or skeletal muscles.

On a clinical examination, there is noticeable reduced resistance to passive movements. The muscles might feel unusually soft to touch. Additionally, diminished deep tendon reflexes might be present.

Treatment and Management[edit | edit source]

The primary management for hypotonia stemming from idiopathic or neurologic causes includes:

  • Physical Therapy: To improve muscle strength and coordination.
  • Occupational Therapy: Aims to enhance fine motor skills and daily living activities.
  • Music Therapy: Can stimulate muscle movement and coordination through rhythm and melodies.

Early intervention is paramount, as it can significantly improve the prognosis and quality of life for those with hypotonia.

Summary[edit | edit source]

Hypotonia is associated with disruptions in the input from stretch receptors or potential abnormalities in the cerebellum's facilitatory influence on the fusimotor system. This system is responsible for controlling muscle spindle sensitivity. While the condition may pose challenges, with timely diagnosis, intervention, and appropriate therapies, individuals with hypotonia can lead productive lives.

External links[edit | edit source]

References[edit | edit source]

Hypotonia Resources



Contributors: Prab R. Tumpati, MD