 |
English
|
正體中文
|
简体中文
|
Items with full text/Total items : 12145/12927 (94%)
Visitors : 905065
Online Users : 839
|
|
|
Loading...
|
Please use this identifier to cite or link to this item:
http://ir.nhri.org.tw/handle/3990099045/3151
|
| Title: | Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion |
| Authors: | Fang, JS;Lee, KF;Huang, CT;Syu, CL;Yang, KJ;Wang, LH;Liao, DL;Chen, CH |
| Contributors: | Division of Mental Health and Substance Abuse Research |
| Abstract: | Terminal or interstitial deletion on the short arm of chromosome 5 is associated with a genetic disorder, cri-du-chat syndrome (cat cry syndrome), which is characterized by a cat-like cry in infancy, facial dysmorphism, microcephaly, and mental retardation. There is a high degree of variation in clinical presentations of patients with cri-du-chat syndrome, which is usually associated with different sizes and locations of deletions in chromosome 5p. Most patients with a 5p deletion have de novo mutations; familial 5p deletion is rare in literature. Here, we report a three-generation family with a 5p terminal deletion. The terminal 5p deletion (5p15.2-pter) in this family was confirmed and characterized by karyotyping analysis, fluorescent in situ hybridization, array comparative genome hybridization, and quantitative polymerase chain reaction. Although the affected family members apparently share deletions of the same size, there are some variations in mental symptoms within this family. Two affected females manifest moderate mental retardation and psychotic symptoms such as delusion of persecution, auditory hallucination, self-talking, and self-laughing, which are rare in cri-du-chat syndrome. In contrast, the other three affected males express mild-to-moderate mental retardation but no psychotic symptoms. Our study suggests that other factors besides the size and location of 5p deletions may modify the mental presentations of patients with 5p deletions. |
| Keywords: | Genetics & Heredity |
| Date: | 2008-06 |
| Relation: | Clinical Genetics. 2008 Jun;73(6):585-590. |
| Link to: | http://dx.doi.org/10.1111/j.1399-0004.2008.00995.x |
| JIF/Ranking 2023: | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0009-9163&DestApp=IC2JCR |
| Cited Times(WOS): | https://www.webofscience.com/wos/woscc/full-record/WOS:000255819000012 |
| Cited Times(Scopus): | http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=43449089496 |
| Appears in Collections: | [陳嘉祥(2009-2013)] 期刊論文
[廖定烈(2005-2008)] 期刊論文
|
Files in This Item:
| File |
Description |
Size | Format | |
|---|
| 000255819000012.pdf | | 407Kb | Adobe PDF | 1151 | View/Open |
|
All items in NHRI are protected by copyright, with all rights reserved.
|
