Mirror movements (MM) are contralateralinvoluntary movements that mirror vol-untary ones. MM are occasionally found in young children, but persistence beyond age 10 is unusual except in certain disorders of nervous sys-tem crossing such as Klippel-Feil and Kallmann syndrome. The study of individuals with MM can provide important insights into the mechanisms of contralateral innervation. We recently described a large four-generation French Canadian (FC) family with isolated congen-italMM (CMM) (1). Pedigree analysis suggested autosomal dominant inheritance with incomplete penetrance. We conducted a genome-wide link-age analysis and identified a single significant locus on chromosome 18q21.2. Haplotype analysis indi-cated that all affected in...
Patients with Kallmann’s syndrome show hypothalamic hypogonadism, hyposmia, and congenital mirror mo...
L'objectif de mon travail a été d'étudier les bases génétiques de deux maladies du mouvement, les mo...
Background: Moebius syndrome is a rare disorder with minimum clinical criteria of congenital facial ...
International audienceBACKGROUND: Autosomal dominant congenital mirror movements (CMM) is a neurodev...
Objective: We screened a large series of individuals with congenital mirror movements (CMM) for muta...
Summary: We describe a case of hereditary congenital mirror movements (MMs) in a 76-year-old man, wh...
International audienceCongenital mirror movements (CMM) disorder is characterized by involuntary mov...
Congenital mirror movements (CMM) are characterized by involuntary movements of one side of the body...
© 2018, Logos Medical Publishing. All rights reserved.Coexistence of Klippel Feil syndrome, Poland s...
Mirror movements are involuntary movements that occur in homologous contralateral muscles on volunta...
Mirror movement is a rare condition and refers to involuntary movements that occur in homologous con...
International audienceBackground. Mirror movements are involuntary movements of one hand that mirror...
Dystroglycanopathies are a heterogeneous group of muscular dystrophies often associated with variabl...
Mirror movements are involuntary symmetrical movements of one side of the body that mirror voluntary...
Patients with Kallmann's syndrome show hypothalamic hypogonadism, hyposmia, and congenital mirror mo...
Patients with Kallmann’s syndrome show hypothalamic hypogonadism, hyposmia, and congenital mirror mo...
L'objectif de mon travail a été d'étudier les bases génétiques de deux maladies du mouvement, les mo...
Background: Moebius syndrome is a rare disorder with minimum clinical criteria of congenital facial ...
International audienceBACKGROUND: Autosomal dominant congenital mirror movements (CMM) is a neurodev...
Objective: We screened a large series of individuals with congenital mirror movements (CMM) for muta...
Summary: We describe a case of hereditary congenital mirror movements (MMs) in a 76-year-old man, wh...
International audienceCongenital mirror movements (CMM) disorder is characterized by involuntary mov...
Congenital mirror movements (CMM) are characterized by involuntary movements of one side of the body...
© 2018, Logos Medical Publishing. All rights reserved.Coexistence of Klippel Feil syndrome, Poland s...
Mirror movements are involuntary movements that occur in homologous contralateral muscles on volunta...
Mirror movement is a rare condition and refers to involuntary movements that occur in homologous con...
International audienceBackground. Mirror movements are involuntary movements of one hand that mirror...
Dystroglycanopathies are a heterogeneous group of muscular dystrophies often associated with variabl...
Mirror movements are involuntary symmetrical movements of one side of the body that mirror voluntary...
Patients with Kallmann's syndrome show hypothalamic hypogonadism, hyposmia, and congenital mirror mo...
Patients with Kallmann’s syndrome show hypothalamic hypogonadism, hyposmia, and congenital mirror mo...
L'objectif de mon travail a été d'étudier les bases génétiques de deux maladies du mouvement, les mo...
Background: Moebius syndrome is a rare disorder with minimum clinical criteria of congenital facial ...