Dell'Osso L F
Jpn J Ophthalmol. 1985;29(4):351-68.
Patients with congenital types of nystagmus, including congenital nystagmus (CN), latent/manifest latent nystagmus (LMLN) and combinations of the two, can be identified by waveform analysis and classified into three unambiguous groups. This categorization by waveform is supported by different clinical signs, including the relationship to strabismus. Strabismus is essential for LMLN but incidental to CN; most CN patients do not have strabismus. Seventy-seven percent of CN patients have a convergence null, 57% a gaze angle null and nearly half have both; only 14% have neither. Also supporting this patient grouping by waveform is the high incidence of patients in each of the two major groups (ie, they had either only CN waveforms or only the LMLN waveform). Comparing the incidence of each CN waveform, or combinations of waveforms, in families with that in the general CN population, reveals that heredity plays a role in determining waveform; heredity also affects other characteristics, such as gaze angle or convergence nulls. The nystagmus blockage syndrome has at least two mechanisms and the patients, therefore, can belong to either of two groups. Spasmus nutans is hypothesized to be an oscillation of the vergence system and therefore, unrelated to CN or LMLN.
患有先天性眼球震颤类型的患者,包括先天性眼球震颤(CN)、潜伏性/显性潜伏性眼球震颤(LMLN)以及两者的组合,可以通过波形分析进行识别,并分为三个明确的组。这种基于波形的分类得到了不同临床体征的支持,包括与斜视的关系。斜视对于LMLN至关重要,但对于CN来说是偶然出现的;大多数CN患者没有斜视。77%的CN患者有集合性消除,57%有凝视角度消除,近一半患者两者都有;只有14%两者都没有。两个主要组中每组患者的高发病率也支持这种基于波形的患者分组(即他们要么只有CN波形,要么只有LMLN波形)。将有家族史的患者中每种CN波形或波形组合的发病率与一般CN人群中的发病率进行比较,发现遗传在决定波形方面起作用;遗传也会影响其他特征,如凝视角度或集合性消除。眼球震颤阻滞综合征至少有两种机制,因此,患者可以属于两个组中的任何一组。痉挛性斜颈被推测为辐辏系统的一种振荡,因此,与CN或LMLN无关。