Difference between revisions of "Craniofacial anomalies"

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*[[Sotos Syndrome]]
 
*[[Sotos Syndrome]]
 
*[[Treacher Collins Syndrome]]
 
*[[Treacher Collins Syndrome]]
 +
1q terminal deletion
 +
Aarskog-Scott syndrome
 +
Al Gazali Aziz Salem syndrome
 +
Barber-Say syndrome
 +
Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia
 +
Chromosome 22 Ring
 +
Chromosome 5, monosomy 5q35
 +
Congenital rubella syndrome
 +
Congenital syphilis
 +
Cri du chat syndrome
 +
DiGeorge syndrome
 +
Fetal alcohol syndrome
 +
Frints -- De Smet -- Fabry -- Fryns syndrome
 +
Gloomy face syndrome
 +
Laurence-Moon-Biedl syndrome
 +
Microphthalmia syndromic, type 9
 +
Multiple joint dislocations -- metaphyseal dysplasia
 +
Noonan syndrome
 +
Pfeiffer syndrome Type 2
 +
Polysyndactyly -- cardiac malformation
 +
Riddle syndrome
 +
Turner syndrome
 +
Valproic acid antenatal infection
 +
Vitiligo mental retardation facial dysmorphism uremia
 +
Williams Syndrome
 +
Young-Simpson syndrome
  
 
==Causes==
 
==Causes==
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{{Reflist|2}}
 
{{Reflist|2}}
  
[[Category:Signs and symptoms]]
+
 
 +
[[Category:FLK]]

Latest revision as of 13:28, 3 June 2015

WikiDoc Resources for Craniofacial anomalies

Articles

Most recent articles on Craniofacial anomalies

Most cited articles on Craniofacial anomalies

Review articles on Craniofacial anomalies

Articles on Craniofacial anomalies in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Craniofacial anomalies

Images of Craniofacial anomalies

Photos of Craniofacial anomalies

Podcasts & MP3s on Craniofacial anomalies

Videos on Craniofacial anomalies

Evidence Based Medicine

Cochrane Collaboration on Craniofacial anomalies

Bandolier on Craniofacial anomalies

TRIP on Craniofacial anomalies

Clinical Trials

Ongoing Trials on Craniofacial anomalies at Clinical Trials.gov

Trial results on Craniofacial anomalies

Clinical Trials on Craniofacial anomalies at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Craniofacial anomalies

NICE Guidance on Craniofacial anomalies

NHS PRODIGY Guidance

FDA on Craniofacial anomalies

CDC on Craniofacial anomalies

Books

Books on Craniofacial anomalies

News

Craniofacial anomalies in the news

Be alerted to news on Craniofacial anomalies

News trends on Craniofacial anomalies

Commentary

Blogs on Craniofacial anomalies

Definitions

Definitions of Craniofacial anomalies

Patient Resources / Community

Patient resources on Craniofacial anomalies

Discussion groups on Craniofacial anomalies

Patient Handouts on Craniofacial anomalies

Directions to Hospitals Treating Craniofacial anomalies

Risk calculators and risk factors for Craniofacial anomalies

Healthcare Provider Resources

Symptoms of Craniofacial anomalies

Causes & Risk Factors for Craniofacial anomalies

Diagnostic studies for Craniofacial anomalies

Treatment of Craniofacial anomalies

Continuing Medical Education (CME)

CME Programs on Craniofacial anomalies

International

Craniofacial anomalies en Espanol

Craniofacial anomalies en Francais

Business

Craniofacial anomalies in the Marketplace

Patents on Craniofacial anomalies

Experimental / Informatics

List of terms related to Craniofacial anomalies

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and Keywords: facial anomalies, CFA, facial dysmorphism

Overview

Craniofacial anomalies are a group of deformities of the head and face that are present at birth.

Classification

Pathophysiology

Associated Disorders

1q terminal deletion Aarskog-Scott syndrome Al Gazali Aziz Salem syndrome Barber-Say syndrome Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia Chromosome 22 Ring Chromosome 5, monosomy 5q35 Congenital rubella syndrome Congenital syphilis Cri du chat syndrome DiGeorge syndrome Fetal alcohol syndrome Frints -- De Smet -- Fabry -- Fryns syndrome Gloomy face syndrome Laurence-Moon-Biedl syndrome Microphthalmia syndromic, type 9 Multiple joint dislocations -- metaphyseal dysplasia Noonan syndrome Pfeiffer syndrome Type 2 Polysyndactyly -- cardiac malformation Riddle syndrome Turner syndrome Valproic acid antenatal infection Vitiligo mental retardation facial dysmorphism uremia Williams Syndrome Young-Simpson syndrome

Causes

Epdidemiology and Demographics

In the United States, craniosynostosis occurs in about 1 in every 2000 births.

Gender

The disorder is more common in boys than in girls.

Treatment

Surgery.

References


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