Hemifacial microsomia with pulmonary hypoplasia
نویسندگان
چکیده
منابع مشابه
Hemifacial microsomia.
Hemifacial microsomia (HFM) is a condition in which the lower half of one side of the face is underdeveloped and does not grow in a normal pattern. After clefts, this is the second most common facial birth defect. Etiology of HFM is unknown, but prenatal exposures of some drugs and genetic abnormalities may be associated with the condition. Diagnosis and treatment of HFM is challenging due to a...
متن کاملA Child with Lung Hypoplasia, Congenital Heart Disease, Hemifacial Microsomia, and Inguinal Hernia: Ipsilateral Congenital Malformations
A 3-year-old Chinese boy was diagnosed with ipsilateral congenital malformations: right lung hypoplasia, dextroversion of heart, atrial septal defect, hepatic vein drainage directly into the right atrium, facial asymmetry, right microtia and congenital deafness, and indirect inguinal hernia. He underwent indirect inguinal hernia repair at the age of 2. Although without any facial plastic surger...
متن کاملNeurodevelopmental outcomes in children with hemifacial microsomia.
OBJECTIVE To determine whether preadolescent children with hemifacial microsomia (HFM) have higher risk of neurodevelopmental delays than unaffected control individuals. DESIGN Case-control follow-up study of neurodevelopment in children with and without HFM. SETTING Case individuals were originally recruited from 26 craniofacial centers across the United States and Canada, and controls wer...
متن کاملPsychosocial outcomes in children with hemifacial microsomia.
OBJECTIVE To determine whether children with hemifacial microsomia (HFM) have higher risk for psychosocial problems than children without HFM. METHODS One hundred and thirty-six children with HFM (64% male, mean age = 6.9 years) were compared to 568 matched controls (50% male, mean age = 7.0 years) on parent and teacher measures of behavior problems and social competence, and teacher rankings...
متن کاملDental agenesis in hemifacial microsomia.
Hemifacial microsomia (HM) is an asymmetrical congenital deformity of the head and face caused by anomalous development of the structures derived from the first and second branchial arches. This study evaluates the incidence of agenesis and dental inclusions in HM patients. Sixty-three HM patients, 27 male and 36 female, ranging from 7 to 43 years had monolateral (61) and bilateral (2) presenta...
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ژورنال
عنوان ژورنال: Case Reports
سال: 2010
ISSN: 1757-790X
DOI: 10.1136/bcr.04.2009.1759