Progressive hemifacial atrophy (Parry‐Romberg syndrome) report with review of genetics and nosology

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Abstract
We describe a boy with mild hemifacial atrophy (Parry‐Romberg syndrome); he had localized scleroderma on a leg and his trunk, and antinuclear antibodies in his serum. These findings support suggestions that this disorder could be a variant of localized scleroderma rather than a developmental anomaly or dysplasia. A review of the literature does not support assertions of autosomal dominant inheritance of the condition.