Literature DB >> 11738838

Three decades of sociomedical experiences from West Swedish Rett females 4-60 years of age.

B Hagberg1, M Berg, U Steffenburg.   

Abstract

Rett syndrome, today known as a worldwide important cause behind severe mental retardation in females, has been seen in Sweden since the 1960s (the senior author). This study gives population representative clinical and sociomedical follow-up data from West Sweden (1/4 of the population in Sweden). The series comprises 54 females diagnosed in 1971-1998, 5-60 years old, median age 20. Mortality in 1971-2000 was 18% (10/54), median age at death 20. Death usually had been sudden and unexpected. The sociomedical follow-up emphasized the adult group. The large majority had usually moved to small group homes, a good and well-accepted environment once the staff had learned the particularities of these so uniquely neurodevelopmentally disabled women.

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Year:  2001        PMID: 11738838     DOI: 10.1016/s0387-7604(01)00331-x

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  4 in total

1.  Describing the phenotype in Rett syndrome using a population database.

Authors:  L Colvin; S Fyfe; S Leonard; T Schiavello; C Ellaway; N De Klerk; J Christodoulou; M Msall; H Leonard
Journal:  Arch Dis Child       Date:  2003-01       Impact factor: 3.791

2.  Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study.

Authors:  Nicky Halbach; Eric E Smeets; Peter Julu; Ingegerd Witt-Engerström; Giorgio Pini; Stefania Bigoni; Stig Hansen; Flora Apartopoulos; Robert Delamont; Kees van Roozendaal; Maria F Scusa; Paolo Borelli; Math Candel; Leopold Curfs
Journal:  Am J Med Genet A       Date:  2016-06-29       Impact factor: 2.802

Review 3.  Key issues in Rett syndrome: emotional, behavioural and autonomic dysregulation (EBAD) - a target for clinical trials.

Authors:  Jatinder Singh; Paramala Santosh
Journal:  Orphanet J Rare Dis       Date:  2018-07-31       Impact factor: 4.123

4.  Increased Mitochondrial Mass and Cytosolic Redox Imbalance in Hippocampal Astrocytes of a Mouse Model of Rett Syndrome: Subcellular Changes Revealed by Ratiometric Imaging of JC-1 and roGFP1 Fluorescence.

Authors:  Dörthe F Bebensee; Karolina Can; Michael Müller
Journal:  Oxid Med Cell Longev       Date:  2017-08-13       Impact factor: 6.543

  4 in total

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