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脊髓性肌萎缩症。

Spinal muscular atrophy.

机构信息

Department of Neurosciences, Unit of Molecular Medicine for Neuromuscular and Neurodegenerative Disorders, Bambino Gesu' Children's Research Hospital, P.za S. Onofrio, 4, Rome (00165), Italy.

出版信息

Orphanet J Rare Dis. 2011 Nov 2;6:71. doi: 10.1186/1750-1172-6-71.

Abstract

Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease characterized by degeneration of alpha motor neurons in the spinal cord, resulting in progressive proximal muscle weakness and paralysis. Estimated incidence is 1 in 6,000 to 1 in 10,000 live births and carrier frequency of 1/40-1/60. This disease is characterized by generalized muscle weakness and atrophy predominating in proximal limb muscles, and phenotype is classified into four grades of severity (SMA I, SMAII, SMAIII, SMA IV) based on age of onset and motor function achieved. This disease is caused by homozygous mutations of the survival motor neuron 1 (SMN1) gene, and the diagnostic test demonstrates in most patients the homozygous deletion of the SMN1 gene, generally showing the absence of SMN1 exon 7. The test achieves up to 95% sensitivity and nearly 100% specificity. Differential diagnosis should be considered with other neuromuscular disorders which are not associated with increased CK manifesting as infantile hypotonia or as limb girdle weakness starting later in life. Considering the high carrier frequency, carrier testing is requested by siblings of patients or of parents of SMA children and are aimed at gaining information that may help with reproductive planning. Individuals at risk should be tested first and, in case of testing positive, the partner should be then analyzed. It is recommended that in case of a request on carrier testing on siblings of an affected SMA infant, a detailed neurological examination should be done and consideration given doing the direct test to exclude SMA. Prenatal diagnosis should be offered to couples who have previously had a child affected with SMA (recurrence risk 25%). The role of follow-up coordination has to be managed by an expert in neuromuscular disorders and in SMA who is able to plan a multidisciplinary intervention that includes pulmonary, gastroenterology/nutrition, and orthopedic care. Prognosis depends on the phenotypic severity going from high mortality within the first year for SMA type 1 to no mortality for the chronic and later onset forms.

摘要

脊髓性肌萎缩症(SMA)是一种常染色体隐性神经肌肉疾病,其特征是脊髓中的α运动神经元退化,导致进行性近端肌肉无力和瘫痪。估计发病率为每 6000 至 10000 例活产儿中有 1 例,携带者频率为 1/40-1/60。这种疾病的特征是广泛的肌肉无力和萎缩,主要影响近端肢体肌肉,表型根据发病年龄和获得的运动功能分为四个严重程度等级(SMA I、SMAII、SMAIII、SMA IV)。这种疾病是由生存运动神经元 1(SMN1)基因的纯合突变引起的,诊断测试在大多数患者中显示 SMN1 基因的纯合缺失,通常表现为 SMN1 外显子 7 的缺失。该测试的灵敏度高达 95%,特异性接近 100%。应考虑与其他不伴有 CK 升高的神经肌肉疾病进行鉴别诊断,这些疾病表现为婴儿期肌无力或生命后期出现肢体带肌无力。鉴于高携带者频率,患者的兄弟姐妹或 SMA 患儿的父母要求进行携带者检测,目的是获得可能有助于生殖计划的信息。应首先对风险个体进行检测,如果检测结果阳性,则应分析其伴侣。建议在请求对 SMA 患病婴儿的兄弟姐妹进行携带者检测时,应进行详细的神经系统检查,并考虑进行直接检测以排除 SMA。对于之前有 SMA 患儿的夫妇,应提供产前诊断(复发风险 25%)。随访协调的角色应由神经肌肉疾病和 SMA 方面的专家来管理,该专家能够计划多学科干预,包括肺、胃肠病学/营养和矫形护理。预后取决于表型严重程度,从 1 型 SMA 的高死亡率到慢性和后期发病形式的无死亡率不等。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbb5/3231874/623a2334a335/1750-1172-6-71-1.jpg

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