Background: Moebius syndrome is a rare disorder with minimum clinical criteria of congenital facial weakness in association with impairment in abduction of one or both eyes. Mirror movements are not known to be associated with Moebius syndrome. Case Report: We present three patients who meet minimum criteria for a diagnosis of Moebius syndrome and who also display mirror movements. Discussion: This case series suggests that Moebius syndrome may be associated with mirror movements. Further investigation to delineate the genetic etiologies of Moebius syndrome is ongoing. Patients with Moebius syndrome and mirror movements may represent a specific subclass of this disorder
Moebius syndrome, a rare congenital disorder of varying severity, involves multiple cranial nerves a...
Pervasive developmental disorders are neuropsychiatric disorders that start in early years of life, ...
THE following case of persistent mirror-movements is interesting from several points of view. Althou...
Background: Moebius syndrome is a rare disorder with minimum clinical criteria of congenital facial ...
Moebius syndrome is an extremely rare disorder. Only approximately few hundred cases have been repor...
Moebius syndrome is a congenital malformation of the brainstem that is non-progressive typically cau...
Moebius Syndrome (MBS) is a rare neurodevelopmental disorder characterised by facial paralysis and o...
Mirror movement is a rare condition and refers to involuntary movements that occur in homologous con...
Mirror movements are involuntary movements that occur in homologous contralateral muscles on volunta...
Mirror movements are involuntary movements that occur in homologous contralateral muscles on volunta...
Mirror movements (MMs) are specifically defined as involuntary movements occurring on one side of ho...
Congenital mirror movements are rare conditions that define the inability to perform unimanual movem...
The diagnosis of Moebius syndrome, a rare congenital disorder, is primarily based on congenital faci...
Moebius syndrome is usually sporadic. The few familial cases reported in the literature have autosom...
Summary: We describe a case of hereditary congenital mirror movements (MMs) in a 76-year-old man, wh...
Moebius syndrome, a rare congenital disorder of varying severity, involves multiple cranial nerves a...
Pervasive developmental disorders are neuropsychiatric disorders that start in early years of life, ...
THE following case of persistent mirror-movements is interesting from several points of view. Althou...
Background: Moebius syndrome is a rare disorder with minimum clinical criteria of congenital facial ...
Moebius syndrome is an extremely rare disorder. Only approximately few hundred cases have been repor...
Moebius syndrome is a congenital malformation of the brainstem that is non-progressive typically cau...
Moebius Syndrome (MBS) is a rare neurodevelopmental disorder characterised by facial paralysis and o...
Mirror movement is a rare condition and refers to involuntary movements that occur in homologous con...
Mirror movements are involuntary movements that occur in homologous contralateral muscles on volunta...
Mirror movements are involuntary movements that occur in homologous contralateral muscles on volunta...
Mirror movements (MMs) are specifically defined as involuntary movements occurring on one side of ho...
Congenital mirror movements are rare conditions that define the inability to perform unimanual movem...
The diagnosis of Moebius syndrome, a rare congenital disorder, is primarily based on congenital faci...
Moebius syndrome is usually sporadic. The few familial cases reported in the literature have autosom...
Summary: We describe a case of hereditary congenital mirror movements (MMs) in a 76-year-old man, wh...
Moebius syndrome, a rare congenital disorder of varying severity, involves multiple cranial nerves a...
Pervasive developmental disorders are neuropsychiatric disorders that start in early years of life, ...
THE following case of persistent mirror-movements is interesting from several points of view. Althou...