Craniofacial anomalies

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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