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Ectrodactyly in a Chinese patient born to a mother with neuromyelitis optica spectrum disorder
Journal article   Open access   Peer reviewed

Ectrodactyly in a Chinese patient born to a mother with neuromyelitis optica spectrum disorder

Y. Chang, Y. Shu, X. Sun, C. Xu, D. He, L. Fang, C. Chen, X. Hu, A. Kermode and W. Qiu
Multiple Sclerosis and Related Disorders, Vol.19, pp.70-72
2018
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Abstract

NMOSD develops primarily in women of childbearing age, and several previous studies have shown that the disorder may increase the risk of miscarriage. However, there are no reports, to our knowledge, of fetal malformation, other than neonatal hydrocephalus, related to NMOSD. We report a 30-year-old woman who experienced recurrent neuritis and who was seropositive for AQP4-IgG. She became pregnant, and the fetus was found to have ectrodactyly. Histological analysis of the placenta showed moderate inflammatory infiltration; however, whether fetal malformation in NMOSD is related to inflammation and AQP4-IgG remains to be determined.

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Collaboration types
Domestic collaboration
International collaboration
Citation topics
1 Clinical & Life Sciences
1.203 Neuromuscular Disorders
1.203.147 Multiple Sclerosis
Web Of Science research areas
Clinical Neurology
ESI research areas
Neuroscience & Behavior
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