TY - JOUR
T1 - A longitudinal study of neurological soft signs from late childhood into early adulthood
AU - Martins, Isabel
AU - Lauterbach, Martin
AU - Slade, Peter
AU - Luís, Henriques
AU - Derouen, Timothy
AU - Martin, Michael
AU - Caldas, Alexandre
AU - Leitão, Jorge
AU - Rosenbaum, Gail
AU - Townes, Brenda
PY - 2008
Y1 - 2008
N2 - Neurological examination of children includes the screening for soft neurological signs (NSS). There is little knowledge about their evolution during adolescence, except that their lasting presence has been associated with developmental, psychological, and cognitive disorders. We report the results of a NSS exam (assessing gross and fine motor function and the presence of hyperactivity and motor impersistence) over a 5-year period, among a group of healthy children who were followed annually as part of a dental study. Their ages ranged from 11 to 15 years at onset to 14 to 18 years at the end. Participants were divided into four groups by age (younger and older) and sex. At the first evaluation there were 191 males and 150 females. NSS score diminished both with increasing age and follow-up time in both groups, but at different rates in males and females. Females reached the lowest scores two years before the younger subgroup of males. These results show that NSS change rapidly in adolescence and at different rates in males and females, which must be taken into account in clinical contexts. The evolution of NSS suggests that they are a signature of neural development.
AB - Neurological examination of children includes the screening for soft neurological signs (NSS). There is little knowledge about their evolution during adolescence, except that their lasting presence has been associated with developmental, psychological, and cognitive disorders. We report the results of a NSS exam (assessing gross and fine motor function and the presence of hyperactivity and motor impersistence) over a 5-year period, among a group of healthy children who were followed annually as part of a dental study. Their ages ranged from 11 to 15 years at onset to 14 to 18 years at the end. Participants were divided into four groups by age (younger and older) and sex. At the first evaluation there were 191 males and 150 females. NSS score diminished both with increasing age and follow-up time in both groups, but at different rates in males and females. Females reached the lowest scores two years before the younger subgroup of males. These results show that NSS change rapidly in adolescence and at different rates in males and females, which must be taken into account in clinical contexts. The evolution of NSS suggests that they are a signature of neural development.
UR - http://www.scopus.com/inward/record.url?scp=48749085457&partnerID=8YFLogxK
U2 - 10.1111/j.1469-8749.2008.03043.x
DO - 10.1111/j.1469-8749.2008.03043.x
M3 - Article
C2 - 18754898
AN - SCOPUS:48749085457
SN - 0012-1622
VL - 50
SP - 602
EP - 607
JO - Developmental Medicine and Child Neurology
JF - Developmental Medicine and Child Neurology
IS - 8
ER -