Zea Vera Alonso, Bruce Adrienne, Larsh Travis R, Jordan Zachary, Brüggemann Norbert, Westenberger Ana, Espay Alberto J, Gilbert Donald L, Wu Steve W
Department of Neurology Children's National Hospital Washington DC USA.
Department of Neurology George Washington University School of Medicine & Health Sciences Washington DC USA.
Mov Disord Clin Pract. 2022 Dec 23;10(2):316-322. doi: 10.1002/mdc3.13635. eCollection 2023 Feb.
pathogenic variants are associated with hypomyelination, hypodontia, hypogonadism, and movement disorders.
We describe the range of movement disorders seen in six patients (four female, two male) with variants [three novel (c.2214del, c.3775G>A, c.3905G>T) and six previously reported (c.760C>T, c.1771-7C>G, c.1909+22G>A, c.2005C>T, c.2422C>T, c.3337-11T>C)]. Patient 1 presented with a neonatal progeroid syndrome and developed parkinsonism, dystonia, ataxia, and spasticity. Patient 2 presented with infant-onset rapidly progressive chorea, and dystonia. Three patients (patients 3, 5, 6) presented predominantly with ataxia in combination with spasticity and dystonia. Patient 4 developed segmental dystonia during adolescence and ataxia in early adulthood. Four patients had vertical gaze impairment. The most common brain MRI abnormality was T2-weighted/FLAIR hyperintensity of the superior cerebellar peduncles and midbrain.
-related disorders exhibit significant phenotypic pleomorphism. Vertical gaze dysfunction and T2-weighted/FLAIR hyperintensity of the superior cerebellar peduncles and midbrain may be useful signs suggestive of this condition.
致病变异与髓鞘形成不足、牙齿发育不全、性腺功能减退和运动障碍有关。
我们描述了6例携带变异(3种新变异[c.2214del、c.3775G>A、c.3905G>T]和6种先前报道的变异[c.760C>T、c.1771-7C>G、c.1909+22G>A、c.2005C>T、c.2422C>T、c.3337-11T>C])患者(4名女性,2名男性)出现的一系列运动障碍。患者1表现为新生儿早老综合征,并出现帕金森症、肌张力障碍、共济失调和痉挛。患者2表现为婴儿期起病的快速进展性舞蹈症和肌张力障碍。3名患者(患者3、5、6)主要表现为共济失调,伴有痉挛和肌张力障碍。患者4在青春期出现节段性肌张力障碍,成年早期出现共济失调。4名患者有垂直凝视障碍。最常见的脑部MRI异常是小脑上脚和中脑的T2加权/液体衰减反转恢复序列高信号。
相关疾病表现出显著的表型多态性。垂直凝视功能障碍以及小脑上脚和中脑的T2加权/液体衰减反转恢复序列高信号可能是提示该病的有用体征。