Literature DB >> 9383025

Applicability of a checklist for clinical screening of the fragile X syndrome.

M Arvio1, M Peippo, K O Simola.   

Abstract

In a population of 340,000 in Southern Häme, Finland, there were 541 intellectually disabled adult males (> 16 years) known to the District Organisation for the Care of the Mentally Retarded in August 1993. Of these, 197 already had a confirmed etiological diagnosis, with 20 having the fragile X syndrome. The other 344 males were screened for the fragile X syndrome using a three-step method: a clinical checklist used by a specialist nurse, a clinical examination by a physician who was very familiar with the fragile X syndrome, and the FRAXA-locus gene test. Six new fragile X males were found. The minimum prevalence of the fragile X syndrome in the district was calculated to be 1:4400.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9383025     DOI: 10.1111/j.1399-0004.1997.tb02549.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  6 in total

1.  Screening for the fragile X syndrome among the mentally retarded: a clinical study. The Collaborative Fragile X Study Group.

Authors:  B B de Vries; S Mohkamsing; A M van den Ouweland; E Mol; K Gelsema; M van Rijn; A Tibben; D J Halley; H J Duivenvoorden; B A Oostra; M F Niermeijer
Journal:  J Med Genet       Date:  1999-06       Impact factor: 6.318

Review 2.  The fragile X syndrome.

Authors:  B B de Vries; D J Halley; B A Oostra; M F Niermeijer
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

Review 3.  FMR1 and the fragile X syndrome: human genome epidemiology review.

Authors:  D C Crawford; J M Acuña; S L Sherman
Journal:  Genet Med       Date:  2001 Sep-Oct       Impact factor: 8.822

4.  Common Clinical Characteristics and Rare Medical Problems of Fragile X Syndrome in Thai Patients and Review of the Literature.

Authors:  Chariyawan Charalsawadi; Juthamas Wirojanan; Somchit Jaruratanasirikul; Nichara Ruangdaraganon; Alan Geater; Pornprot Limprasert
Journal:  Int J Pediatr       Date:  2017-06-29

5.  Signs indicating dementia in Down, Williams and Fragile X syndromes.

Authors:  Oili Sauna-Aho; Nina Bjelogrlic-Laakso; Auli Siren; Maria Arvio
Journal:  Mol Genet Genomic Med       Date:  2018-07-03       Impact factor: 2.183

6.  Fragile X checklists: A meta-analysis and development of a simplified universal clinical checklist.

Authors:  Toni Kasole Lubala; Aimé Lumaka; Gray Kanteng; Léon Mutesa; Olivier Mukuku; Stanislas Wembonyama; Randi Hagerman; Oscar Numbi Luboya; Prosper Lukusa Tshilobo
Journal:  Mol Genet Genomic Med       Date:  2018-04-06       Impact factor: 2.183

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.