Background: Rett Syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized by developmental regression, particularly in relation to expressive language and use of the hands. It is also associated with profound mental retardation and almost exclusively affects females.Case Details: A four and a half year old girl reported to our dental OPD for a dental checkup. On complete examination, she was diagnosed to be suffering from Rett Syndrome. Preventive therapies and proper oral hygiene instructions were explained to her mother.Conclusion: Early diagnosis of such disorders is extremely important along with treatment of patients’ problems with love and care to prevent them from further pain and stress.Keyowrds: Rett Syndr...
The purpose of this paper is to explore the causes, characteristics, and interventions associated w...
Abstract The overlap between autism and Rett syndrome clinical features has led to many cases of Ret...
Rett syndrome (RTT), a neurodevelopmental condition characterized by delayed-onset loss of spoken la...
Rett syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized by developme...
AbstractRett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the...
From November 1982 to May 1999, 28 children with Rett syndrome were followed-up for a medium period ...
Rett syndrome is a mental retardation syndrome that occurs only in females and consists of normal pr...
Rett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the gene en...
[[abstract]]Rett syndrome (RTT), a neurodevelopmental condition characterized by delayed-onset loss ...
The purpose of this paper is to inform readers of what classic Rett syndrome is and what can be don...
Background: Rett syndrome, a common cause of mental retardation in females, is caused by mutations ...
Rett syndrome (RS), a neurological developmental disor-der, is one of the commonest causes of cognit...
Rett syndrome (RTT), a neurodevelopmental condition characterized by delayed-onset loss of spoken la...
Rett syndrome, a neurodegenerative disorder, occurs almost exclusively in female children and has an...
PubMed ID: 10204460Rett syndrome is a unique and puzzling disorder noted in females and is possibly ...
The purpose of this paper is to explore the causes, characteristics, and interventions associated w...
Abstract The overlap between autism and Rett syndrome clinical features has led to many cases of Ret...
Rett syndrome (RTT), a neurodevelopmental condition characterized by delayed-onset loss of spoken la...
Rett syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized by developme...
AbstractRett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the...
From November 1982 to May 1999, 28 children with Rett syndrome were followed-up for a medium period ...
Rett syndrome is a mental retardation syndrome that occurs only in females and consists of normal pr...
Rett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the gene en...
[[abstract]]Rett syndrome (RTT), a neurodevelopmental condition characterized by delayed-onset loss ...
The purpose of this paper is to inform readers of what classic Rett syndrome is and what can be don...
Background: Rett syndrome, a common cause of mental retardation in females, is caused by mutations ...
Rett syndrome (RS), a neurological developmental disor-der, is one of the commonest causes of cognit...
Rett syndrome (RTT), a neurodevelopmental condition characterized by delayed-onset loss of spoken la...
Rett syndrome, a neurodegenerative disorder, occurs almost exclusively in female children and has an...
PubMed ID: 10204460Rett syndrome is a unique and puzzling disorder noted in females and is possibly ...
The purpose of this paper is to explore the causes, characteristics, and interventions associated w...
Abstract The overlap between autism and Rett syndrome clinical features has led to many cases of Ret...
Rett syndrome (RTT), a neurodevelopmental condition characterized by delayed-onset loss of spoken la...