| Literature DB >> 27712809 |
Abstract
There are thousands of craniofacial disorders, each with a different etiology. All cases of orofacial clefts have an underlying genetic cause, ranging from multifactorial with an underlying genetic predisposition to chromosomal and single-gene etiologies. More than 50% of cases of Pierre Robin sequence are syndromic and 25% of craniosynostoses are syndromic. Clinical genetics evaluation is important for each patient with a craniofacial condition to make a proper diagnosis, counsel the family, and assist in management. This is an overview of the major components of the clinical genetics evaluation with a review of many syndromes associated with craniofacial disorders.Entities:
Keywords: Cleft lip; Cleft palate; Dysmorphology; Family history; Genetic counseling; Genetic evaluation; Genetic testing; Teratogens
Mesh:
Year: 2016 PMID: 27712809 DOI: 10.1016/j.fsc.2016.06.001
Source DB: PubMed Journal: Facial Plast Surg Clin North Am ISSN: 1064-7406 Impact factor: 1.918