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Handwringing in Rett syndrome: a normal developmental stage.
1Department of Pediatrics, UCLA School of Medicine.
Pediatric Neurology
|May 1, 1992
Summary
Handwringing in Rett syndrome emerges after hand function loss, often mistaken for stress. This repetitive behavior is actually a key indicator of severe apraxia in affected individuals.
Area of Science:
- Neurology
- Developmental Pediatrics
Background:
- Handwringing is a hallmark clinical manifestation in Rett syndrome.
- This behavior typically emerges following the loss of hand function in affected individuals.
- Normal hand development in infants includes grasping, but this progresses minimally in Rett syndrome.
Purpose of the Study:
- To differentiate the significance of handwringing in Rett syndrome from its occurrence in typical infant development.
- To highlight the underlying apraxia masked by distressed behaviors during Rett syndrome onset.
- To clarify the diagnostic confusion arising from handwringing as both a stress response and a symptom of neurological impairment.
Main Methods:
- Clinical observation of hand movements in Rett syndrome patients.
- Comparison of hand behaviors in Rett syndrome with normal infant developmental milestones.
- Analysis of the relationship between hand function, apraxia, and behavioral symptoms.
Main Results:
- Original hand function in Rett syndrome rarely progresses beyond basic grasping.
- Handwringing in Rett syndrome appears after the loss of functional hand use.
- Handwringing and hand mouthing are transient, normal stages in 14-week-old infants.
Conclusions:
- Handwringing in Rett syndrome is a critical sign of severe apraxia, not merely a stress response.
- The onset of distressed behavior can misdirect clinical attention from the core issue of apraxia.
- Distinguishing pathological handwringing from normal developmental behaviors is crucial for accurate diagnosis and management of Rett syndrome.