منابع مشابه
Orthognathic Surgery in Craniofacial Microsomia: Treatment Algorithm
Craniofacial microsomia is a broad term that covers a variety of craniofacial malformation conditions that are caused by alterations in the derivatives of the first and second pharyngeal arches. In general terms, diverse therapeutic alternatives are proposed according to the growth stage and the severity of the alteration. When craniofacial growth has concluded, conventional orthognathic surger...
متن کامل1 Converse : Chapter 54 Craniofacial Microsomia
Among the congenital otocephalic syndromes, the term "first and second branchial arch syndrome" designates, in the United States, a characteristic congenital malformation which is usually unilateral but occasionally bilateral. In the German literature, the deformity has been termed "dysostosis otomandibularis". Caronni (1971) has coined the term "auriculobranchiogenic dysplasia". Stark and Saun...
متن کاملPhotographic protocol for image acquisition in craniofacial microsomia
Craniofacial microsomia (CFM) is a congenital condition associated with orbital, mandibular, ear, nerve, and soft tissue anomalies. We present a standardized, two-dimensional, digital photographic protocol designed to capture the common craniofacial features associated with CFM.
متن کاملCraniofacial Microsomia: Goldenhar Syndrome in Association with Bilateral Congenital Cataract
Craniofacial microsomia (CFM) includes a spectrum of malformations primarily involving structures derived from the first and second branchial arches. Patients with hemifacial microsomia and epibulbar dermoids are said to have Goldenhar syndrome (GHS). Four-month-old boy with whitish pupillary reflex presented with the features of GHS in pediatric ophthalmology clinic. The child had ocular and a...
متن کاملGenome-wide association study identifies multiple susceptibility loci for craniofacial microsomia
Craniofacial microsomia (CFM) is a rare congenital anomaly that involves immature derivatives from the first and second pharyngeal arches. The genetic pathogenesis of CFM is still unclear. Here we interrogate 0.9 million genetic variants in 939 CFM cases and 2,012 controls from China. After genotyping of an additional 443 cases and 1,669 controls, we identify 8 significantly associated loci wit...
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ژورنال
عنوان ژورنال: Seminars in Plastic Surgery
سال: 2012
ISSN: 1535-2188,1536-0067
DOI: 10.1055/s-0032-1320067