Hemifacial Microsomia
What is hemifacial microsomia (HFM)?
Hemifacial microsomia (HFM) is a condition in which the tissue on one side of the face is underdeveloped, affecting primarily the aural (ear), oral (mouth), and mandibular (jaw) areas.
Hemifacial microsomia
Disease Information
Overview In-Depth Tests Treatment
& Care Contact Us ...
Hemifacial microsomia: See: Goldenhar syndrome.
Search All of MedicineNet For:
Privacy Policy ...
hemifacial microsomia (Also called Goldenhar syndrome, brachial arch syndrome, facio-auriculo-vertebral syndrome, oculo-auriculo-vertebral spectrum, or lateral facial dysplasia.) - a condition in which the tissues on one side of the face are ...
Hemifacial Microsomia
Detailed information on hemifacial microsomia, including types, causes, diagnosis, and treatment
Home Page - Craniofacial Anomalies ...
hemifacial microsomia-a condition in which the tissues on one side of the face are underdeveloped, affecting primarily the ear (aural), mouth (oral), and jaw (mandibular) areas.
Further low-frequency findings include facial asymmetry (hemifacial microsomia), external ear malformations, lung lobation defects, intestinal malrotation and genital anomalies. VATER/VACTERL features are more common in twinning.
Anatomy of the Newborn Skull
Deformational Plagiocephaly
Glossary - Craniofacial Anomalies
Hemifacial Microsomia ...
in syndromic patients and children with conditions such as cleft palate, severe asymmetry, severe mandibular hypoplasia with resulting airway compromise, facial clefts, Treacher-Collins syndrome, Pierre-Robin sequence and hemifacial microsomia.
 See also: Craniofacial Anomalies, Surgery, Anatomy, Cleft palate, Cleft lip
  
|
RSS
