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扩展先天性肌病谱:产前发病伴颈部极度过伸。

Expanding the spectrum of congenital myopathies: prenatal onset with extreme hyperextension of the neck.

机构信息

Neonatology Unit, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.

Neonatal Intensive Care Unit, Medical and Surgical Department of Fetus, Newborn and Infant, Bambino Gesù Children's Hospital IRCCS, Rome, Italy.

出版信息

Neurol Sci. 2021 Apr;42(4):1549-1553. doi: 10.1007/s10072-020-04937-x. Epub 2020 Nov 26.

Abstract

We describe the case of a male newborn presenting with a prenatal diagnosis of persistent hyperextension of the fetal neck and severe hypotonia and respiratory insufficiency at birth. Facial weakness, increased serum creatine kinase levels, and abnormal feeding, together with other signs, such as severe contractures, also classically associated with congenital myopathies prompted to perform a muscle biopsy showing internal rods suggestive of a possible nemaline myopathy. These findings suggest that a careful neurological examination should be performed in infants with persistent hyperextension of the fetal neck to exclude weakness and a possible underlying muscle disorder.

摘要

我们描述了一名男性新生儿的病例,该患儿产前诊断为胎儿颈部持续过度伸展,出生时伴有严重的肌张力低下和呼吸功能不全。面部无力、血清肌酸激酶水平升高以及喂养异常等其他症状,加上严重的挛缩等也与先天性肌病有关,促使我们进行了肌肉活检,结果显示有内部杆状结构,提示可能为杆状体肌病。这些发现表明,对于存在胎儿颈部持续过度伸展的婴儿,应进行仔细的神经学检查,以排除肌无力和可能存在的肌肉疾病。

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