2007
DOI: 10.1016/j.bjoms.2007.07.133
|View full text |Cite
|
Sign up to set email alerts
|

Congenital anomalies associated with cleft lip and palate

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
1
0
1

Year Published

2008
2008
2008
2008

Publication Types

Select...
2
1

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(2 citation statements)
references
References 0 publications
0
1
0
1
Order By: Relevance
“…This malformation is involved in more than 100 syndromes, and trisomy 13 is the most frequently associated chromosomal anomaly3. In one recent series of 1623 patients with CLP, 15% had associated malformations, which were most frequent in patients with unilateral involvement of the lip and palate (37%), followed in decreasing order by isolated cleft palate (23%), bilateral CLP (20%), cleft lip with or without cleft alveolar ridge (17%), and submucosal cleft (3%)4. The most frequent location of associated malformations is the facial region (21%), followed by the ocular system, central nervous system, skeletal system, cardiovascular system, neck, auricular system, gastrointestinal system and urogenital system.…”
Section: Introductionmentioning
confidence: 99%
“…This malformation is involved in more than 100 syndromes, and trisomy 13 is the most frequently associated chromosomal anomaly3. In one recent series of 1623 patients with CLP, 15% had associated malformations, which were most frequent in patients with unilateral involvement of the lip and palate (37%), followed in decreasing order by isolated cleft palate (23%), bilateral CLP (20%), cleft lip with or without cleft alveolar ridge (17%), and submucosal cleft (3%)4. The most frequent location of associated malformations is the facial region (21%), followed by the ocular system, central nervous system, skeletal system, cardiovascular system, neck, auricular system, gastrointestinal system and urogenital system.…”
Section: Introductionmentioning
confidence: 99%
“…La mayoría de los genes relacionados con las FOF forma sindrómica tienen un papel esencial en el desarrollo del tejido conectivo y por esta razón las alteraciones congénitas que más frecuentemente están asociadas a esta entidad son las que afectan el sistema musculoesquelético. (Hwang, et al, 1998, Sekhon, et al, 2011, Mossey, et al, 2012. Este estudio es evidencia de lo anterior, pues además de ser este el sistema que más frecuentemente se ve afectado, en lo que anomalías congénitas se refiere; la DDC, una patología del tejido conectivo presenta una asociación estadísticamente significativa con las FOF sindrómicas.…”
Section: Discussionunclassified