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Postnatal-onset microcephaly: pathogenesis, patterns of growth, and prediction of outcome
N Paul Rosman1, Daniel C Tarquinio, Marianna Datseris
1Department of Pediatrics, Division of Pediatric Neurology, Boston Medical Center, Boston University School of Medicine, Boston, Massachusetts 02118, USA. npaul.rosman@bmc.org
Insights
Children with postnatal-onset microcephaly (POM) often have poor development. However, better body growth, including weight, height, and head circumference, predicts more favorable developmental outcomes in these children.
Area of Science:
- Pediatric Neurology
- Developmental Pediatrics
- Clinical Genetics
Background:
- Postnatal-onset microcephaly (POM) is associated with significant developmental challenges in affected children.
- Understanding factors that influence developmental trajectories in POM is crucial for early intervention and prognosis.
Purpose of the Study:
- To investigate the relationship between somatic growth parameters (weight, height, head circumference) and developmental quotient (DQ) in children with POM.
- To identify predictors of neurodevelopmental outcomes in a cohort of children diagnosed with POM.
Main Methods:
- A longitudinal study followed 57 children with POM (encephaloclastic, dysgenetic, Rett syndrome, idiopathic) for an average of 4.2 years.
- Developmental quotient (DQ) was assessed regularly; SD scores for weight, height, and head circumference were analyzed using mixed-effects models.
- Pearson's correlation examined the independent influence of growth parameters on final DQ.
Main Results:
- 77% of children with POM exhibited a low DQ; however, 23% achieved normal DQ, predominantly in the idiopathic group.
- Mean head circumference fell below -2 SDS before age 1 year in all etiological subgroups.
- Weight, height, and head circumference were significant independent predictors of DQ (P < .0001), with height showing the strongest correlation (r = 0.41).
Conclusions:
- While most children with POM experience poor development, sustained postnatal growth is linked to more favorable outcomes.
- Approximately one-quarter of children with POM, particularly those with idiopathic causes, can achieve normal developmental quotients.
- Somatic growth parameters serve as important indicators for predicting developmental trajectories in children with POM.
Objective:
Although children with postnatal-onset microcephaly (POM) generally have poor development, we speculated that better somatic growth would predict better development in these children.
Patients And Methods:
We followed 57 children with POM for an average of 4.2 years (13 encephaloclastic, 14 dysgenetic, 6 with Rett syndrome, 24 idiopathic) and calculated the developmental quotient (DQ) at each visit (DQ > 0.70 was considered normal). SD scores (SDS) for measurements were analyzed using a repeated measures mixed-effects model to assess effect of weight, height, head circumference (HC), and age on DQ. Pearson's correlation was used to examine the independent influence of each variable on final DQ.
Results:
Forty-four children (77%) had a low DQ (mean: 0.33), but 13 (23%) had a normal DQ (mean: 0.93), including 10 idiopathic and 3 encephaloclastic. Mean HC fell below -2 SDS in all before 1 year (destructive at 3.3 months, idiopathic low-DQ at 7.5 months, dysgenetic at 8.5 months, Rett syndrome at 11 months, and idiopathic normal-DQ at 11.5 months). Mean weights and heights both fell below -2 SDS for all low-DQ groups but remained normal in both normal-DQ groups. Weight, height, and HC were independent predictors of DQ (P < .0001). Final DQ correlated with weight (r = 0.27), height (r = 0.41), and HC (r = 0.13).
Conclusions:
Most children with POM have poor later development. Whatever the cause of POM, persons in whom postnatal body growth (weight, height, HC) is better sustained have more favorable development, and in one-quarter of such persons (mostly idiopathic POM), final DQ is normal.
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