Williams Syndrome with a “Twist”
Joint Authors
Maritsi, Despoina N.
Vartzelis, George
Kossiva, Lydia
Source
Issue
Vol. 2010, Issue 2010 (31 Dec. 2010), pp.1-2, 2 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2010-06-16
Country of Publication
Egypt
No. of Pages
2
Main Subjects
Abstract EN
Williams syndrome is a rare genetic condition with multisystemic involvement, caused by a microscopic deletion in the chromosome band 7q11.23.
We describe the first case of a toddler with Williams syndrome who developed Benign Paroxysmal Torticollis (BPT), a benign dystonic disorder of unknown aetiology.
American Psychological Association (APA)
Maritsi, Despoina N.& Kossiva, Lydia& Vartzelis, George. 2010. Williams Syndrome with a “Twist”. Case Reports in Medicine،Vol. 2010, no. 2010, pp.1-2.
https://search.emarefa.net/detail/BIM-493790
Modern Language Association (MLA)
Maritsi, Despoina N.…[et al.]. Williams Syndrome with a “Twist”. Case Reports in Medicine No. 2010 (2010), pp.1-2.
https://search.emarefa.net/detail/BIM-493790
American Medical Association (AMA)
Maritsi, Despoina N.& Kossiva, Lydia& Vartzelis, George. Williams Syndrome with a “Twist”. Case Reports in Medicine. 2010. Vol. 2010, no. 2010, pp.1-2.
https://search.emarefa.net/detail/BIM-493790
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-493790
