Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Home
Search
Quick Search
Advanced
Fulltext
Browse
Collections
Persons
My eDoc
Session History
Login
Name:
Password:
Documentation
Help
Support Wiki
Direct access to
document ID:


          Institute: MPI für molekulare Genetik     Collection: Department of Human Molecular Genetics     Display Documents



  history
ID: 194741.0, MPI für molekulare Genetik / Department of Human Molecular Genetics
D4F104S1 deletion in facioscapulohumeral muscular dystrophy - Phenotype, size, and detection
Authors:Lemmers, R. J. L. F.; Osborn, M.; Haaf, Thomas; Rogers, M.; Frants, R. R.; Padberg, G. W.; Cooper, D. N.; van der Maarel, S. M.; Upadhyaya, M.
Language:English
Date of Publication (YYYY-MM-DD):2003-07-22
Title of Journal:Neurology
Journal Abbrev.:Neurology
Volume:61
Issue / Number:2
Start Page:178
End Page:183
Copyright:© 2003 American Academy of Neurology
Review Status:not specified
Audience:Experts Only
Abstract / Description:Background:
The facioscapulohumeral muscular dystrophy (FSHD) locus maps to 4q35 where it is closely linked to D4F104S1 (p13E-11), a probe that recognizes the pathognomonic FSHD deletion involving the subtelomeric D4Z4 tandem repeat array. Extended deletions that include both the more proximal D4F104S1 region and the D4Z4 repeat array proper do, however, occur, albeit rarely, and such deletions can lead to difficulties of interpretation in the diagnostic setting.
Objective:
To devise a means to determine the true frequency of proximally extended deletions in individuals with FSHD.
Methods:
Three families selected for this study were originally identified during routine FSHD analysis on the basis that the affected individuals in each family had failed to exhibit a small (<38-kb) EcoRI fragment. High molecular weight DNA from these families was analyzed with both conventional and pulsed-field gel electrophoresis using DNA markers p13E-11, 9B6A, B31, 4qA, and 4qB.
Results:
Large genomic deletions were identified involving both D4Z4 and D4F104S1. The precise number of D4Z4 repeat units borne by the p13E11 deletion allele was established by the use of an additional restriction enzyme (MseI) digest. All three cases carry different sizes of deletion proximal to the D4Z4 repeat units. With use of a recently described telomeric probe, 4qA, a method was developed that identifies large genomic deletions involving both D4Z4 and D4F104S1 using conventional gel electrophoresis.

Conclusion: Proximally extended deletions can be found in patients with a normal spectrum of the disease. This assay promises to allow estimation of the true frequency of proximally extended deletions and should improve the accuracy and reliability of molecular diagnostic testing for FSHD.
Comment of the Author/Creator:Date: 2003, JUL 22
External Publication Status:published
Document Type:Article
Version Comment:Automatic journal name synchronization
Communicated by:Hans-Hilger Ropers
Affiliations:MPI für molekulare Genetik
External Affiliations:Univ Wales Coll Med, Inst Med Genet, Cardiff CF14 4XN, S Glam, Wales.; Leiden Univ, Med Ctr, Ctr Human & Clin Genet, Dept Human Genet, NL-2333 AL Leiden, Netherlands.; Univ Med Ctr Nijmegen, Dept Neurol, Nijmegen, Netherlands.; Babraham Inst, Dept Mol Immunol, Cambridge, England.; Max Planck Inst Mol Genet, Berlin, Germany.
Identifiers:ISI:000184281800009 [ID No:1]
ISSN:0028-3878 [ID No:2]
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.