Hemifacial Microsomia: Symptoms, Causes & Treatment - Cleveland Clinic
2024年11月11日 · Hemifacial microsomia (craniofacial microsomia) is a condition you’re born with. It occurs when features on one side of your face don’t develop as they should. It most commonly occurs on one side of your face but can sometimes affect both sides (bilateral hemifacial microsomia).
Hemifacial Microsomia | National Institute of Dental and …
Changes in the face can sometimes be seen in an ultrasound during pregnancy, and the physician may suspect hemifacial microsomia before birth. However, doctors usually diagnose hemifacial microsomia by examining the face after the baby is born.
Hemifacial Microsomia - Children's Hospital of Philadelphia
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 areas, though it may also involve the eye, cheek, neck, and other parts of the skull, as well as nerves and soft tissue.
Hemifacial Microsomia - Johns Hopkins Medicine
What is hemifacial microsomia? Hemifacial microsomia is a common congenital facial difference that causes asymmetric development of the face. Hemifacial has been called many terms such as Goldenhar syndrome and oculo-auriculo-vertebral spectrum. They are all the same condition.
Hemifacial Microsomia (HFM) in Children
Hemifacial microsomia (HFM) is a congenital disorder. This means that your child is born with it. In this condition, one side of your baby’s face is underdeveloped (hemi means half). HFM usually only affects one side of the face. Sometimes both sides may be affected.
Hemifacial Microsomia (HFM) in Children | UMass Memorial Health
What is hemifacial microsomia in children? Hemifacial microsomia (HFM) is a congenital problem. This means that your child is born with it. In this condition, one side of your baby’s face is underdeveloped. (Hemi means half). HFM usually only affects one side of the face. Sometimes both sides may be affected.
Hemifacial microsomia - Wikipedia
Hemifacial microsomia (HFM) is a congenital disorder that affects the development of the lower half of the face, most commonly the ears, the mouth and the mandible. It usually occurs on one side of the face, but both sides are sometimes affected.
Hemifacial Microsomia - Boston Children's Hospital
Most children with hemifacial microsomia have a significantly underdeveloped upper and/or lower jaw. This can lead to difficulty chewing and keeping the teeth properly aligned. The treatment depends on the extent of your child’s symptoms.
Hemifacial Microsomia (HFM) in Children - Health Encyclopedia ...
Hemifacial microsomia (HFM) is a congenital problem. This means that your child is born with it. In this condition, one side of your baby’s face is underdeveloped.
Hemifacial Microsomia - Children's National Hospital
Hemifacial microsomia (HFM) is a congenital problem. This means that your child is born with it. In this condition, one side of your baby’s face is underdeveloped ("hemi" means half). HFM usually only affects one side of the face. Sometimes both sides may be affected.
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