Congenital absence of salivary glands in Down syndrome
Background Children with Down syndrome have different saliva composition compared to normal children. The presence or absence of the salivary glands has not been previously reported. Objective To examine the presence or absence of the salivary glands in children with Down syndrome. Methods 15 childr...
Saved in:
Published in: | Archives of disease in childhood Vol. 98; no. 10; pp. 781 - 783 |
---|---|
Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
London
BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health
01-10-2013
BMJ Publishing Group BMJ Publishing Group Ltd BMJ Publishing Group LTD |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Background Children with Down syndrome have different saliva composition compared to normal children. The presence or absence of the salivary glands has not been previously reported. Objective To examine the presence or absence of the salivary glands in children with Down syndrome. Methods 15 children with Down syndrome underwent an ultrasound examination of the salivary glands. The control group consisted of 31 healthy children. The areas of the parotid and submandibular glands on both sides were scanned in an attempt to demonstrate all four glands. The result was reported as ‘present’ or ‘absent’. Results In four children out of 15 with Down syndrome, one or more salivary glands were absent (26.7%), while in the controls all salivary glands were present. The difference between the groups was statistically significant (p=0.008). There was no significant difference between the groups regarding age and sex. Conclusions At least one salivary gland is undetected by ultrasound in some children with Down syndrome. |
---|---|
Bibliography: | ArticleID:archdischild-2013-303841 local:archdischild;98/10/781 href:archdischild-98-781.pdf PMID:23908188 ark:/67375/NVC-8XPM23CK-L istex:FDD185EA689633ED5534CC503B3786060F6F366B ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0003-9888 1468-2044 |
DOI: | 10.1136/archdischild-2013-303841 |