Craniofacial Abnormalities

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Basics

Summary
Treatments and Therapies

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Related Issues
Specifics
Genetics

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Summary

Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft lip and palate, are among the most common of all birth defects. Others are very rare. Most of them affect how a person's face or head looks. These conditions may also affect other parts of the body.

Treatment depends on the type of problem. Plastic and reconstructive surgery may help the person's appearance.

Treatments and Therapies

Craniofacial reconstruction - slideshow (Medical Encyclopedia) Also in Spanish

Related Issues

Baby's Head Shape: What's Normal? (Mayo Foundation for Medical Education and Research) Also in Spanish
Empowering Children to Cope with Teasing (Children's Craniofacial Association) - PDF

Specifics

Coffin Lowry Syndrome (National Institute of Neurological Disorders and Stroke)
Craniosynostosis (Mayo Foundation for Medical Education and Research)
Craniosynostosis (National Institute of Neurological Disorders and Stroke)
Flat Head Syndrome (Positional Plagiocephaly) (Nemours Foundation) Also in Spanish
Guide to Understanding Apert Syndrome (Children's Craniofacial Association) - PDF
Guide to Understanding Hemifacial Microsomia (Children's Craniofacial Association) - PDF
Guide to Understanding Pfeiffer Syndrome (Children's Craniofacial Association) - PDF
Holoprosencephaly (National Institute of Neurological Disorders and Stroke)
Learning about Holoprosencephaly (HPE) (National Human Genome Research Institute)
Noonan Syndrome: Symptoms and Causes (Mayo Foundation for Medical Education and Research)
Sotos Syndrome (National Institute of Neurological Disorders and Stroke)
Treacher Collins Syndrome (Cleft Palate Foundation)

Genetics

Genetics Home Reference: 3MC syndrome (National Library of Medicine)
Genetics Home Reference: Aarskog-Scott syndrome (National Library of Medicine)
Genetics Home Reference: acrocallosal syndrome (National Library of Medicine)
Genetics Home Reference: Apert syndrome (National Library of Medicine)
Genetics Home Reference: Baller-Gerold syndrome (National Library of Medicine)
Genetics Home Reference: Beare-Stevenson cutis gyrata syndrome (National Library of Medicine)
Genetics Home Reference: blepharocheilodontic syndrome (National Library of Medicine)
Genetics Home Reference: Bohring-Opitz syndrome (National Library of Medicine)
Genetics Home Reference: Bosma arhinia microphthalmia syndrome (National Library of Medicine)
Genetics Home Reference: Bowen-Conradi syndrome (National Library of Medicine)
Genetics Home Reference: branchio-oculo-facial syndrome (National Library of Medicine)
Genetics Home Reference: Burn-McKeown syndrome (National Library of Medicine)
Genetics Home Reference: cardiofaciocutaneous syndrome (National Library of Medicine)
Genetics Home Reference: Carpenter syndrome (National Library of Medicine)
Genetics Home Reference: cherubism (National Library of Medicine)
Genetics Home Reference: cleidocranial dysplasia (National Library of Medicine)
Genetics Home Reference: craniofacial microsomia (National Library of Medicine)
Genetics Home Reference: craniometaphyseal dysplasia (National Library of Medicine)
Genetics Home Reference: Crouzon syndrome (National Library of Medicine)
Genetics Home Reference: Crouzon syndrome with acanthosis nigricans (National Library of Medicine)
Genetics Home Reference: enlarged parietal foramina (National Library of Medicine)
Genetics Home Reference: frontonasal dysplasia (National Library of Medicine)
Genetics Home Reference: Fryns syndrome (National Library of Medicine)
Genetics Home Reference: Gorlin-Chaudhry-Moss syndrome (National Library of Medicine)
Genetics Home Reference: Greig cephalopolysyndactyly syndrome (National Library of Medicine)
Genetics Home Reference: Hartsfield syndrome (National Library of Medicine)
Genetics Home Reference: isolated Pierre Robin sequence (National Library of Medicine)
Genetics Home Reference: Jackson-Weiss syndrome (National Library of Medicine)
Genetics Home Reference: mandibulofacial dysostosis with microcephaly (National Library of Medicine)
Genetics Home Reference: Miller syndrome (National Library of Medicine)
Genetics Home Reference: Muenke syndrome (National Library of Medicine)
Genetics Home Reference: Nager syndrome (National Library of Medicine)
Genetics Home Reference: oral-facial-digital syndrome (National Library of Medicine)
Genetics Home Reference: Pfeiffer syndrome (National Library of Medicine)
Genetics Home Reference: Robinow syndrome (National Library of Medicine)
Genetics Home Reference: Saethre-Chotzen syndrome (National Library of Medicine)
Genetics Home Reference: Shprintzen-Goldberg syndrome (National Library of Medicine)
Genetics Home Reference: Simpson-Golabi-Behmel syndrome (National Library of Medicine)
Genetics Home Reference: Sotos syndrome (National Library of Medicine)
Genetics Home Reference: thanatophoric dysplasia (National Library of Medicine)
Genetics Home Reference: Treacher Collins syndrome (National Library of Medicine)
Genetics Home Reference: Weaver syndrome (National Library of Medicine)

Clinical Trials

ClinicalTrials.gov: Craniofacial Abnormalities (National Institutes of Health)
ClinicalTrials.gov: Craniosynostoses (National Institutes of Health)

Journal Articles References and abstracts from MEDLINE/PubMed (National Library of Medicine)

Find an Expert

Children

What Is Treacher Collins Syndrome? (for Parents) (Nemours Foundation)

Patient Handouts

Apert syndrome (Medical Encyclopedia) Also in Spanish
Cleidocranial dysostosis (Medical Encyclopedia) Also in Spanish
Craniosynostosis (Medical Encyclopedia) Also in Spanish
Craniosynostosis repair (Medical Encyclopedia) Also in Spanish
Head and face reconstruction (Medical Encyclopedia) Also in Spanish
Pierre Robin syndrome (Medical Encyclopedia) Also in Spanish