What is Hemifacial Microsomia? Hemifacial Microsomia is a condition in which the lower half of one side of the face is underdeveloped and does not grow.
Hemifacial microsomia is a congenital condition in which the tissues on one side of the face are underdeveloped. It primarily affects the ear, mouth and jaw.
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.
Hemifacial microsomia occurs when part of the face appears small or underdeveloped. Read more on causes of this disorder and how it's treated.
In craniofacial microsomia (CFM), part of the face is smaller than normal Hemifacial microsomia; First and second branchial arch syndrome; Otomandibular.
Hemifacial microsomia is a condition in which half of one side of the face is underdeveloped and does not grow normally. Learn more from Boston Children's .
The severity of hemifacial microsomia varies widely from person to person, but the ear and lower jaw are always affected. When both sides of the face are.
Hemifacial microsomia treatment might involve multiple rounds of hemifacial microsomia surgery. Learn about hemifacial microsomia (HFM) causes and.
Hemifacial microsomia (HM) is a congenital craniofacial malformation caused by hypoplasia of anatomical structures deriving from the first and.
Hemifacial microsomia (HFM) is a congenital disorder. This means that your child is born with it. In this condition, 1 side of your baby's face is underdeveloped.