Ettala-Ylitalo U M, Laine T
Department of Prosthodontics, University of Helsinki, Finland.
Arch Oral Biol. 1991;36(3):189-94. doi: 10.1016/0003-9969(91)90085-9.
In the sample of 208 children, clinical signs and symptoms of craniomandibular disorder were mild, somewhat more common in boys than in girls, and clearly more common in children referred for speech therapy than in the control group. Of variables measured in millimetres, the differences indicate sexual dimorphism rather than differences between boys and girls in the occurrence of craniomandibular disorders. The differences may also reflect later maturing of neuromuscular control in boys rather than true differences between boys and girls in the prevalence of craniomandibular disorder. Logistical regression showed that children with articulatory speech disorders had more subjective symptoms and retrusive interferences, smaller maximal opening, and larger maximal laterotrusion and protrusion movements of the mandible than the controls. Thus different dysfunctions of the orofacial region tend to coexist in the same individuals. Subjective symptoms and clinical signs are mild in 6-8-yr-old children and may reflect immaturity of fine motor control.
在208名儿童的样本中,颅下颌紊乱的临床体征和症状较为轻微,在男孩中比在女孩中更为常见,并且在接受言语治疗转诊的儿童中明显比在对照组中更为常见。在以毫米为单位测量的变量中,差异表明存在性别二态性,而非男孩和女孩在颅下颌紊乱发生率上的差异。这些差异也可能反映出男孩神经肌肉控制成熟较晚,而非男孩和女孩在颅下颌紊乱患病率上的真正差异。逻辑回归分析显示,与对照组相比,患有构音障碍的儿童有更多主观症状和后缩干扰,最大开口度较小,下颌最大侧方运动和前伸运动较大。因此,口面部区域的不同功能障碍往往在同一个体中共存。6至8岁儿童的主观症状和临床体征较为轻微,可能反映出精细运动控制的不成熟。