Javascript must be enabled to continue!
Rett Syndrome
View through CrossRef
Rett syndrome is a common developmental-neurologic disorder that has been reported almost exclusively in females. Recent work has improved recognition of this condition and helped to clarify the management of this disorder for affected individuals. The primary-care physician can become a major source of support and advocacy for the family of a girl with Rett syndrome. Many other resources are available to the primary care giver and the families of children with Rett syndrome; these may help to provide early diagnosis, psychological support, and preventive medical care for these individuals. The current state of knowledge regarding Rett syndrome is reviewed and a framework is provided for medical and developmental interventions.
Title: Rett Syndrome
Description:
Rett syndrome is a common developmental-neurologic disorder that has been reported almost exclusively in females.
Recent work has improved recognition of this condition and helped to clarify the management of this disorder for affected individuals.
The primary-care physician can become a major source of support and advocacy for the family of a girl with Rett syndrome.
Many other resources are available to the primary care giver and the families of children with Rett syndrome; these may help to provide early diagnosis, psychological support, and preventive medical care for these individuals.
The current state of knowledge regarding Rett syndrome is reviewed and a framework is provided for medical and developmental interventions.
Related Results
Atypical Rett syndrome diagnosis by molecular testing
Atypical Rett syndrome diagnosis by molecular testing
Abstract
Rett syndrome is a neurodevelopmental disorder that leads to regression in language and motor skills. In most cases, it is caused by...
Achados neurológicos em estudos de imagem e achados clínicos: revisão de literatura
Achados neurológicos em estudos de imagem e achados clínicos: revisão de literatura
Introdução. A Síndrome de Rett é um distúrbio raro de neurodesenvolvimento, que se caracteriza por perda de habilidades, manifestando-se entre os 6 e 18 meses de idade. O diag...
Mutation Analysis of MECP2 and Clinical Characterization in Korean Patients With Rett Syndrome
Mutation Analysis of MECP2 and Clinical Characterization in Korean Patients With Rett Syndrome
Rett syndrome is a progressive neurodevelopmental disorder occurring predominantly in females. Recently, mutations in the MECP2 gene on Xq28, which encodes methyl-CpG binding prote...
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Abstract
Thoracic outlet syndrome (TOS) is a complex and often overlooked condition caused by the compression of neurovascular structures as they pass through the thoracic outlet. ...
Fregoli Syndrome: A Case Report and Literature Review
Fregoli Syndrome: A Case Report and Literature Review
Abstract
Introduction: Fregoli syndrome is a rare misidentification disorder that can disrupt behavior, endanger safety, and impair quality of life. Its occurrence in young adults ...
Three in One: Systemic Lupus Erythematosus, HELLP Syndrome, and Antiphospholipid Syndrome: A Case Report and Literature Review
Three in One: Systemic Lupus Erythematosus, HELLP Syndrome, and Antiphospholipid Syndrome: A Case Report and Literature Review
Abstract
Introduction
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease commonly affecting women of reproductive age. Its overlap with HELLP syndrome (Hemolysi...
The discriminative role of angiopoietin-like protein-3 for metabolic syndrome in polycystic ovary syndrome
The discriminative role of angiopoietin-like protein-3 for metabolic syndrome in polycystic ovary syndrome
SUMMARY OBJECTIVE: Patients with polycystic ovary syndrome face an increased risk of developing metabolic syndrome. Identifying biomarkers that can detect metabolic syndrome in po...
Features of premorbid status in patients with Rett syndrome
Features of premorbid status in patients with Rett syndrome
Rett syndrome is a severe, progressive developmental condition of the nervous system. It is linked to the X chromosome and affects mainly girls aged 6 to 18 months. The syndrome is...

