Facial bone hyperplasia

Karpagavalli Shanmugasundaram, V. Hemifacial hyperplasia is a rare congenital malformation characterized by noticeable unilateral excess development of hard and soft tissues of the face. The affected side grows exponentially as compared to the unaffected side. Multiple tissue involvement has resulted due to etiological heterogeneity like heredity, chromosomal abnormalities, altered intrauterine environment, and endocrine dysfunctions. As this lesion is rarely seen in our routine clinical practice, we present a case of hemifacial hyperplasia with reported orofacial features that supplement existing clinical knowledge. This paper also adds knowledge to the readers regarding detailed investigation procedures which has complemented our diagnosis.

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Hemifacial hypertrophy

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Orphanet: Hemifacial hyperplasia

Hemifacial hyperplasia is a rare developmental anomaly characterized by marked unilateral facial tissues. It involves orofacial soft tissues, bones of the face, and teeth. The cause remains ambiguous although several predisposing factors have been reported. A case report of a year-old girl with unilateral hemifacial enlargement, pain in temporomandibular joint, and limited mouth opening associated is presented to highlight the clinical and imaging findings and to discuss the differential diagnosis. Hemifacial hyperplasia HFH is a rare congenital developmental disorder characterized by asymmetrical overgrowth of one or more body parts. HFH was initially described by Meckel in and later reported by Wagner in
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Congenital hemifacial hyperplasia

Hemifacial hypertrophy also termed facial hemihypertrophy , [2] facial hemihyperplasia , [2] or Friedreich's disease [3] abbreviated as HFH is rare congenital disease characterized by unilateral enlargement of the head and teeth. Hemifacial hypertrophy can cause a wide spectrum of defects or may involve only muscle or bone. From Wikipedia, the free encyclopedia. Medical condition.
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