Rett syndrome is a developmental and neurological disease characterized by defective X and is caused by mutations in the gene MECP2 coded chromosomes. It is a central involvement diesase that starts in the early developmental years, together along with EEG abnormalities, seizures, mental retardation. Orthopedic, respiratory and cardiac problems can also be seen. Prolonged QT, scoliosis, apnea, cachexia is common in children with this syndrome and requires significant anesthesia care and attention. In this case, we emphasized the anesthetic management of a Rett Syndrome child, its possible risks and problems
AbstractRett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the...
Rett syndrome is a genetic neurodevelopmental disorder that affects mainly girls, but mutations in t...
Rett syndrome (RTT), a neurodevelopmental condition characterized by delayed-onset loss of spoken la...
Rett syndrome is a progressive neurological disorder that occurs only in females and it manifests wi...
Abstract Rett syndrome, which is a progressive, central nervous system disease that is caused by a g...
Rett syndrome (RS) is a neurological disease that occurs onlyin females and it manifests with mental...
Rett syndrome is a childhood neurodevelopmental disorder that affects girls almostt exclusively. It ...
Rett syndrome is characterized by early neurological regression that severely affects motor, cogniti...
Rett syndrome (RTT) is a neurodevelopmental disorder which is characterized by an apparently normal ...
Rett syndrome is one of the most common causes of complex disability in girls. It is characterized b...
Rett syndrome, a neurodegenerative disorder, occurs almost exclusively in female children and has an...
Rett syndrome (RTT, MIM#312750) is a neurodevelopmental disorder that is classified as an autism spe...
Rett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the gene en...
Abstract Background Rett syndrome (RTT) is a severe neurodevelopmental disorder in children characte...
Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder affecting almost exclusively gi...
AbstractRett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the...
Rett syndrome is a genetic neurodevelopmental disorder that affects mainly girls, but mutations in t...
Rett syndrome (RTT), a neurodevelopmental condition characterized by delayed-onset loss of spoken la...
Rett syndrome is a progressive neurological disorder that occurs only in females and it manifests wi...
Abstract Rett syndrome, which is a progressive, central nervous system disease that is caused by a g...
Rett syndrome (RS) is a neurological disease that occurs onlyin females and it manifests with mental...
Rett syndrome is a childhood neurodevelopmental disorder that affects girls almostt exclusively. It ...
Rett syndrome is characterized by early neurological regression that severely affects motor, cogniti...
Rett syndrome (RTT) is a neurodevelopmental disorder which is characterized by an apparently normal ...
Rett syndrome is one of the most common causes of complex disability in girls. It is characterized b...
Rett syndrome, a neurodegenerative disorder, occurs almost exclusively in female children and has an...
Rett syndrome (RTT, MIM#312750) is a neurodevelopmental disorder that is classified as an autism spe...
Rett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the gene en...
Abstract Background Rett syndrome (RTT) is a severe neurodevelopmental disorder in children characte...
Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder affecting almost exclusively gi...
AbstractRett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the...
Rett syndrome is a genetic neurodevelopmental disorder that affects mainly girls, but mutations in t...
Rett syndrome (RTT), a neurodevelopmental condition characterized by delayed-onset loss of spoken la...