Literature DB >> 4061760

Rett syndrome: report of eight cases.

S Rolando.   

Abstract

The author reports eight cases of the Rett syndrome, or dementia-ataxia-autism, in girls. The cases satisfy the following criteria: Normal development in the first mos of life. Profound deterioration of the mental status over a period of several mos. Behavioral pseudoautistic abnormalities. Presence of neurological signs such as ataxia, myoclonus and hyperreflexia. Normal head circumference at birth, but subsequent subnormal growth. EEG abnormalities. Slow progression of the disease after the period of rapid deterioration. The constellation of the signs and symptoms, and the occurrence only in girls, make this clinical picture quite distinct. There is no definitely known biochemical or chromosomal abnormality. The psychological profile, though homogeneous in all the patients, is not pathognomonic, and a very similar behavioral pattern can be observed in other organic brain syndromes.

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Mesh:

Year:  1985        PMID: 4061760     DOI: 10.1016/s0387-7604(85)80030-9

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


  16 in total

Review 1.  Rett syndrome: a review of current knowledge.

Authors:  R Van Acker
Journal:  J Autism Dev Disord       Date:  1991-12

2.  Phenotype Differentiation of FOXG1 and MECP2 Disorders: A New Method for Characterization of Developmental Encephalopathies.

Authors:  Mandy Ma; Heather R Adams; Laurie E Seltzer; William B Dobyns; Alex R Paciorkowski
Journal:  J Pediatr       Date:  2016-09-15       Impact factor: 4.406

3.  Altered expression of neuropeptides in FoxG1-null heterozygous mutant mice.

Authors:  Elisa Frullanti; Sonia Amabile; Maria Grazia Lolli; Anna Bartolini; Gabriella Livide; Elisa Landucci; Francesca Mari; Flora M Vaccarino; Francesca Ariani; Luca Massimino; Alessandra Renieri; Ilaria Meloni
Journal:  Eur J Hum Genet       Date:  2015-05-13       Impact factor: 4.246

4.  FOXG1-Related Disorders: From Clinical Description to Molecular Genetics.

Authors:  C Florian; N Bahi-Buisson; T Bienvenu
Journal:  Mol Syndromol       Date:  2011-04-29

Review 5.  Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature.

Authors:  Francois Dominique Jacob; Vijay Ramaswamy; John Andersen; Francois V Bolduc
Journal:  Eur J Hum Genet       Date:  2009-07-22       Impact factor: 4.246

6.  14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.

Authors:  Carolyn J Ellaway; Gladys Ho; Elisa Bettella; Alisa Knapman; Felicity Collins; Anna Hackett; Fiona McKenzie; Artur Darmanian; Gregory B Peters; Kerry Fagan; John Christodoulou
Journal:  Eur J Hum Genet       Date:  2012-09-12       Impact factor: 4.246

7.  FOXG1 is responsible for the congenital variant of Rett syndrome.

Authors:  Francesca Ariani; Giuseppe Hayek; Dalila Rondinella; Rosangela Artuso; Maria Antonietta Mencarelli; Ariele Spanhol-Rosseto; Marzia Pollazzon; Sabrina Buoni; Ottavia Spiga; Sara Ricciardi; Ilaria Meloni; Ilaria Longo; Francesca Mari; Vania Broccoli; Michele Zappella; Alessandra Renieri
Journal:  Am J Hum Genet       Date:  2008-06-19       Impact factor: 11.025

8.  Hyperventilation in the awake state: potentially treatable component of Rett syndrome.

Authors:  D P Southall; A M Kerr; E Tirosh; P Amos; M H Lang; J B Stephenson
Journal:  Arch Dis Child       Date:  1988-09       Impact factor: 3.791

9.  Rett syndrome: revised diagnostic criteria and nomenclature.

Authors:  Jeffrey L Neul; Walter E Kaufmann; Daniel G Glaze; John Christodoulou; Angus J Clarke; Nadia Bahi-Buisson; Helen Leonard; Mark E S Bailey; N Carolyn Schanen; Michele Zappella; Alessandra Renieri; Peter Huppke; Alan K Percy
Journal:  Ann Neurol       Date:  2010-12       Impact factor: 10.422

10.  iPS cells to model CDKL5-related disorders.

Authors:  Mariangela Amenduni; Roberta De Filippis; Aaron Y L Cheung; Vittoria Disciglio; Maria Carmela Epistolato; Francesca Ariani; Francesca Mari; Maria Antonietta Mencarelli; Youssef Hayek; Alessandra Renieri; James Ellis; Ilaria Meloni
Journal:  Eur J Hum Genet       Date:  2011-07-13       Impact factor: 4.246

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