آنالیز و طرح درمان در بیماران مبتلا به Hemifacial microsomia

نویسنده

  • جعفری, مهدی
چکیده مقاله:

Normal 0 false false false EN-US X-NONE AR-SA Treatment planning for patients with this congenital disorder according to their age, eruption of teeth and anatomical type of the disorder is summarized here. It should be noticed that reconstruction of ear, soft tissue lesions and neurological lesions in patients is done after complete reconstruction of facial bones and functioning of its skeletal parts. /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal" mso-tstyle-rowband-size:0 mso-tstyle-colband-size:0 mso-style-noshow:yes mso-style-priority:99 mso-style-qformat:yes mso-style-parent:"" mso-padding-alt:0cm 5.4pt 0cm 5.4pt mso-para-margin-top:0cm mso-para-margin-right:0cm mso-para-margin-bottom:10.0pt mso-para-margin-left:0cm line-height:115% mso-pagination:widow-orphan font-size:11.0pt font-family:"Calibri","sans-serif" mso-ascii-font-family:Calibri mso-ascii-theme-font:minor-latin mso-hansi-font-family:Calibri mso-hansi-theme-font:minor-latin mso-bidi-font-family:Arial mso-bidi-theme-font:minor-bidi}

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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...

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Dental 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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Treatment of Hemifacial Microsomia: A Case Report

Introduction: Hemifacial microsomia (HFM) is a branchial arch syndrome and the second most common craniofacial birth defect after cleft lip and palate. This syndrome involves the facial skeleton and ear. The most important goal in treatment of HFM is to improve facial symmetry. Traditionally, segment repositioning and costochondral graft were used for the correction of mandibular asymmetry but ...

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Neurodevelopmental 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...

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Characterization of facial paresis in hemifacial microsomia.

OBJECTIVE To provide an overview of the incidence, characteristics, and proposed etiologic mechanisms of facial paresis in patients with manifestations of hemifacial microsomia. DATA SOURCES PubMed database for English-language studies with no date restrictions. REVIEW METHODS A comprehensive literature review was performed identifying all studies that discussed incidence, characterization,...

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عنوان ژورنال

دوره 5  شماره None

صفحات  74- 83

تاریخ انتشار 1992-08

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