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Case 58 - Congenital Myopathies: Nemaline Myopathy

from Myopathies

Published online by Cambridge University Press:  29 November 2024

Jessica E. Hoogendijk
Affiliation:
University Medical Center Utrecht
Marianne de Visser
Affiliation:
Amsterdam University Medical Center
Pieter A. van Doorn
Affiliation:
Erasmus MC, University Medical Center, Rotterdam
Erik H. Niks
Affiliation:
Leiden University Medical Center
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Summary

After a normal pregnancy without hydramnios, delivery of a healthy-looking girl was uneventful. At four months of age, she had had a respiratory infection and was noted to have a weak cough. At eight months of age she was just able to keep her head in an upright position but was not able to sit unsupported. Her mother admitted that she had not been very active since birth, but there was no progressive muscle weakness and no swallowing difficulty. She was referred to a paediatric neurologist because of a suspected neuromuscular disorder. The parents were healthy and there was no consanguinity.

Type
Chapter
Information
Neuromuscular Disease
A Case-Based Approach
, pp. 240 - 242
Publisher: Cambridge University Press
Print publication year: 2024

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References

Suggested Reading

Ahmed, MI, Iqbal, M, Hussain, N. A structured approach to the assessment of a floppy neonate. J Pediatr Neurosci 2016;11(1):26. doi: 10.4103/1817-1745.181250. PMID: 27195025; PMCID: PMC4862282.CrossRefGoogle Scholar
Laitila, J, Wallgren-Pettersson, C. Recent advances in nemaline myopathy. Neuromuscul Disord 2021;31(10):955967. doi: 10.1016/j.nmd.2021.07.012. Epub 2021 Jul 24. PMID: 34561123.CrossRefGoogle ScholarPubMed
Nicolau, S, Milone M. Sporadic Late-Onset Nemaline Myopathy: Current Landscape. Curr Neurol Neurosci Rep. 2023 Nov;23(11):777–784. doi: 10.1007/s11910-023-01311-0. Epub 2023 Oct 19. PMID: 37856049. Google Scholar
Veneruso, M, Fiorillo, C, Broda, P, et al. The role of muscle biopsy in diagnostic process of infant hypotonia: from clinical classification to the genetic outcome. Front Neurol 2021;12:735488. doi: 10.3389/fneur.2021.735488. PMID: 34675869; PMCID: PMC8523832.CrossRefGoogle Scholar

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