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再谈先天性肌张力减退

Congenital hypotonia revisited.

作者信息

Brooke M H, Carroll J E, Ringel S P

出版信息

Muscle Nerve. 1979 Mar-Apr;2(2):84-100. doi: 10.1002/mus.880020203.

DOI:10.1002/mus.880020203
PMID:397413
Abstract

The definition of neuromuscular diseases affecting infants has depended on factors as various as the rate of progression of the illness, the clinical picture, and, recently, the morphologic peculiarities in the muscle biopsy. A review of the literature suggests that there are discrepancies in the classification of such illnesses, no matter what system is used. In some instances, a single diagnosis seems to include patients with quite separate illnesses, whereas other patients with seemingly identical diseases have been given different diagnoses.

摘要

影响婴儿的神经肌肉疾病的定义取决于多种因素,如疾病的进展速度、临床表现,以及最近肌肉活检中的形态学特征。对文献的回顾表明,无论使用何种系统,此类疾病的分类都存在差异。在某些情况下,单一诊断似乎涵盖了患有截然不同疾病的患者,而其他患有看似相同疾病的患者却被给予了不同的诊断。

相似文献

1
Congenital hypotonia revisited.再谈先天性肌张力减退
Muscle Nerve. 1979 Mar-Apr;2(2):84-100. doi: 10.1002/mus.880020203.
2
The newborn with poor muscle tone.
Semin Perinatol. 1982 Jan;6(1):68-88.
3
Approach to diagnosis in the child with muscle weakness.儿童肌无力的诊断方法。
Pediatr Ann. 1977 Mar;6(3):149-61.
4
[Principles and significance of clinical electromyography].[临床肌电图学的原理与意义]
Wien Med Wochenschr. 1971 Mar 27;121(13):250-5.
5
"Floppy baby" (Oppenheim's disease, amyotonia congenital).
Pediatr Ann. 1977 Mar;6(3):194-202.
6
[Current views on the diagnosis, etiology and genetics of the most frequent non-metabolic congenital myopathies].[关于最常见的非代谢性先天性肌病的诊断、病因及遗传学的当前观点]
Padiatr Grenzgeb. 1983;22(1):27-45.
7
[Neurophysiological diagnosis of neuromuscular diseases].[神经肌肉疾病的神经生理学诊断]
Internist (Berl). 1972 Mar;13(3):81-7.
8
[A diagnostic algorithm--infantile hypotonia (the "flabby" child)].一种诊断算法——婴儿肌张力减退(“松软”儿童)
Pediatrie (Bucur). 1992 Apr-Jun;41(2):85-90.
9
[Problem of amyotrophy].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1983;83(11):1601-11.
10
Pathology of the muscular dystrophies and the congenital nonprogressive myopathies.肌肉营养不良症和先天性非进行性肌病的病理学
Pathol Annu. 1980;15(Pt 1):301-33.

引用本文的文献

1
The Evaluation of Facial Muscles by Surface Electromyography in Very Preterm Infants.极低出生体重儿面部肌肉的表面肌电图评估
Biomedicines. 2022 Nov 14;10(11):2921. doi: 10.3390/biomedicines10112921.
2
Corrigendum: A Systematic Review and Meta-Analysis of the Prevalence of Congenital Myopathy.勘误:先天性肌病患病率的系统评价与荟萃分析
Front Neurol. 2022 Feb 14;13:857959. doi: 10.3389/fneur.2022.857959. eCollection 2022.
3
A Systematic Review and Meta-Analysis of the Prevalence of Congenital Myopathy.先天性肌病患病率的系统评价与荟萃分析
Front Neurol. 2021 Nov 2;12:761636. doi: 10.3389/fneur.2021.761636. eCollection 2021.
4
Labor analgesia with ropivacaine added to clonidine: a randomized clinical trial.罗哌卡因联合可乐定用于分娩镇痛:一项随机临床试验。
Sao Paulo Med J. 2008 Mar 6;126(2):102-6. doi: 10.1590/s1516-31802008000200007.
5
Congenital fibre type disproportion with unusual clinico-pathologic manifestations.
J Neurol Neurosurg Psychiatry. 1983 Feb;46(2):175-82. doi: 10.1136/jnnp.46.2.175.
6
Cytochrome-C-oxidase deficiency in muscles of a floppy infant without mitochondrial myopathy.
J Neurol. 1982;227(4):201-7. doi: 10.1007/BF00313387.
7
The spectrum of the so-called rigid spine syndrome: nosological considerations and report of three female cases.
J Neurol. 1986 Aug;233(4):248-53. doi: 10.1007/BF00314029.
8
Benign congenital hypotonia. A clinical study in 43 children.
Eur J Pediatr. 1987 Jul;146(4):360-4. doi: 10.1007/BF00444937.
9
Progression in nemaline myopathy.杆状体肌病的进展
Acta Neuropathol. 1989;78(5):484-91. doi: 10.1007/BF00687709.
10
Follow-up studies in a case of unusual congenital myopathy, suggestive of nemaline type.对一例不寻常的先天性肌病(提示为杆状体肌病类型)的随访研究。
Acta Neuropathol. 1992;83(4):371-8. doi: 10.1007/BF00713528.