Fetal acetylcholine receptor inactivation syndrome is a rare condition occurring in newborns of myasthenic mothers, characterized by bulbar and facial weakness after recovery from the generalized muscle weakness. Antibodies against fetal subunit of acetylcholine receptor seem to have a pathogenetic role leading to long-lasting injury in vulnerable muscle groups. We report a girl, born to a myasthenic mother, who presented with this peculiar phenotype associated with high titers of antibodies specific to the fetal acetylcholine receptor. Although the infant had partial clinical improvement she died prematurely of aspiration pneumonia. We believe that this is a rare but possibly unrecognized condition that should be considered in newborns with persistent myasthenic features even in asymptomatic mothers, and clinicians should consider supportive intervention to avoid fatal complications.
D'Amico, A., Bertini, E. S., Bianco, F., Papacci, P., Jacobson, L., Vincent, A., Mercuri, E. M., Fetal acetylcholine receptor inactivation syndrome and maternal myasthenia gravis: a case report, <<Neuromuscular disorders : NMD>>, 2012; 22 (6): 546-548. [doi:10.1016/j.nmd.2012.01.002] [http://hdl.handle.net/10807/41310]
Fetal acetylcholine receptor inactivation syndrome and maternal myasthenia gravis: a case report
D'Amico, Adele;Bertini, Enrico Silvio;Bianco, Flaviana;Papacci, Patrizia;Mercuri, Eugenio Maria
2012
Abstract
Fetal acetylcholine receptor inactivation syndrome is a rare condition occurring in newborns of myasthenic mothers, characterized by bulbar and facial weakness after recovery from the generalized muscle weakness. Antibodies against fetal subunit of acetylcholine receptor seem to have a pathogenetic role leading to long-lasting injury in vulnerable muscle groups. We report a girl, born to a myasthenic mother, who presented with this peculiar phenotype associated with high titers of antibodies specific to the fetal acetylcholine receptor. Although the infant had partial clinical improvement she died prematurely of aspiration pneumonia. We believe that this is a rare but possibly unrecognized condition that should be considered in newborns with persistent myasthenic features even in asymptomatic mothers, and clinicians should consider supportive intervention to avoid fatal complications.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.