Minor neurological dysfunction after the onset of puberty: association with perinatal events

R J Soorani-Lunsing1, M Hadders-Algra, H J Huisjes

  • 1Department of Developmental Neurology, University Hospital Groningen, Netherlands.

Insights

Puberty can reduce minor neurological dysfunction (MND) signs in adolescents. However, persistent MND at puberty is linked to perinatal factors and neonatal issues, impacting motor skills and coordination.

Area of Science:

  • Developmental Neuroscience
  • Pediatric Neurology
  • Perinatal Medicine

Background:

  • Minor neurological dysfunction (MND) is a subtle neurodevelopmental condition.
  • The relationship between puberty and the resolution of MND requires further investigation.
  • Understanding the long-term impact of perinatal factors on neurodevelopment is crucial.

Purpose of the Study:

  • To test the hypothesis that puberty is associated with a decrease in minor neurological dysfunction (MND).
  • To investigate whether persisting MND in adolescence is associated with perinatal factors.

Main Methods:

  • Longitudinal follow-up of 174 normal and 172 MND children from the Groningen Perinatal Project.
  • Assessment at 12 to 14 years, with puberty defined by the presence of three or more signs.
  • Analysis of specific MND clusters and their association with perinatal and neonatal factors.

Main Results:

  • At 14 years, 55% of children in the MND group showed resolution of signs, while 45% still exhibited milder forms, particularly those newly entering puberty.
  • Pubertal effects on MND were consistent across both sexes.
  • Persistent MND was associated with neonatal neurological deviancy, lower social class, lower obstetrical optimality score, and male sex.

Conclusions:

  • Puberty plays a role in the resolution of minor neurological dysfunction.
  • Specific types of persistent MND in puberty are linked to adverse perinatal events and neonatal neurological status.
  • Fine motor deficits correlate with neonatal deviancy and social class; choreiform dyskinesia with asphyxia; hypotonia with constitutional factors; and coordination issues with prematurity.

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