Journal article
Authors list: Welcker, S.; Heckmann, M.; Axt-Fliedner, R.; Faas, D.
Publication year: 2013
Pages: 139-143
Journal: Zeitschrift für Geburtshilfe & Neonatologie
Volume number: 217
Issue number: 4
ISSN: 0948-2393
eISSN: 1439-1651
DOI Link: https://doi.org/10.1055/s-0033-1349888
Publisher: Georg Thieme Verlag
Abstract:
Neonatal mysthenia gravis (NMG) is a rare cause of arthrogryposis multiplex congenita (AMC) due to diaplacental transfer of maternal acetylcholine receptors (AChR) antibodies. 2 cases of severe NMG complicated by chronic lung disease and pulmonary arterial hypertension are reported. With respect to the severe course of the index patient, prenatal diagnosis and immunomodulation treatment were offered during the 2(nd) pregnancy. The combination of prenatal immunoadsorption (IA) therapy, administration of intravenous immunoglobulin (IVIG) and prednisolone failed. Failure may be partly explained by immaturity of the infant. However, considering the successful treatment of fetal/neonatal alloimmune thrombocytopenia (AIT) reported in literature, a treatment approach with IVIG doses up to 1-2g/kg per week plus prednisone/prednisolone at a higher dose up to 1mg/kg/d might be more effective.
Citation Styles
Harvard Citation style: Welcker, S., Heckmann, M., Axt-Fliedner, R. and Faas, D. (2013) Prenatal Immunomodulation Treatment in Neonatal Myasthenia Gravis, Zeitschrift für Geburtshilfe & Neonatologie, 217(4), pp. 139-143. https://doi.org/10.1055/s-0033-1349888
APA Citation style: Welcker, S., Heckmann, M., Axt-Fliedner, R., & Faas, D. (2013). Prenatal Immunomodulation Treatment in Neonatal Myasthenia Gravis. Zeitschrift für Geburtshilfe & Neonatologie. 217(4), 139-143. https://doi.org/10.1055/s-0033-1349888
Keywords
acetylcholine receptors antibodies; arthrogryposis multiplex congenita; ARTHROGRYPOSIS MULTIPLEX CONGENITA; IMMUNOADSORPTION; IVIG; MATERNAL ANTIBODIES; Neonatal mysthenia gravis; prenatal immunomodulation treatment