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Expanding the MYOD1 Phenotype: A Case Report of a Patient Diagnosed Whilst Pregnant
Journal article   Peer reviewed

Expanding the MYOD1 Phenotype: A Case Report of a Patient Diagnosed Whilst Pregnant

Catherine Ashton, Mark Davis, Merrilee Needham and Phillipa Lamont
Journal of neuromuscular diseases, Vol.9(5), pp.615-618
2022
PMID: 35754284

Abstract

Clinical Neurology Life Sciences & Biomedicine Neurosciences Neurosciences & Neurology Science & Technology
A 38-year-old pregnant woman presented at 30 weeks gestation in respiratory distress with pre-eclampsia. This was on the background of slowly progressive dyspnoea over six years, with generalised weakness and previous surgery for ptosis and prognathia. After successful caesarean delivery at 31 weeks, the patient was found to have a homozygous likely pathogenic variant in the MYOD1 gene. This case presents a milder phenotype for MYOD1 congenital myopathy, usually associated with diaphragmatic defects, respiratory insufficiency and dysmorphic facies. It also highlights the difficulties of managing an undiagnosed patient through pregnancy.

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Collaboration types
Domestic collaboration
Citation topics
1 Clinical & Life Sciences
1.255 Musculoskeletal Disorders
1.255.628 Duchenne Muscular Dystrophy
Web Of Science research areas
Clinical Neurology
Neurosciences
ESI research areas
Neuroscience & Behavior
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