Facial deformities left hand side

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Congenital hemifacial hyperplasia CHH is a rare congenital malformation characterized by marked unilateral overdevelopment of hard and soft tissues of the face. Asymmetry in CHH is usually evident at birth and accentuated with age, especially at puberty. The affected side grows at a rate proportional to the nonaffected side so that the disproportion is maintained thr oughout the life. Multisystem involvement has resulted in etiological heterogeneity including heredity, chromosomal abnormalities, atypical forms of twinning, altered intrauterine environment, and endocrine dysfunctions; however, no single theory explains the etiology adequately. Deformities of all tissues of face, including teeth and their related tissues in the jaw, are key findings for correct diagnosis of CHH.
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Parry–Romberg syndrome is a rare disease characterized by progressive shrinkage and face. Half of these cases are associated with abnormalities in both the gray and white matter of the brain—usually ipsilateral but sometimes The condition is observed on the left side of the face about as often as on the right side. We hereby report a patient having marked left-sided facial atrophy and wasting [1] It is a chronic disorder leading to facial deformity and can be associated with.
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This 6-year-old girl demonstrates the typical characteristics of hemifacial microsomia. Frontal A and lateral B views demonstrate facial asymmetry and severe microtia with aural atresia. The chin point is deviated toward the right, with an upward cant of the ipsilateral commissure and nasal alar base. The facial soft tissue is less prominent on the right side.
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The defect joins a long list of ailments — including smallpox, heart illness and depression — that modern doctors have diagnosed in Lincoln. Ronald Fishman, who led the study published in the August issue of the Archives of Ophthalmology. His facial defect, diagnosed by modern doctors, can be treated by surgery today. When Lincoln was a boy, he was kicked in the head by a horse. The scanning technique is usually used to create 3-D images of children with cleft lip and palate before and after surgery.
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    Parry—Romberg syndrome also known as progressive hemifacial atrophy is a rare disease characterized by progressive shrinkage and degeneration of the tissues beneath the skin , usually on only one side of the face hemifacial atrophy but occasionally extending to other parts of the body.

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