Scleroderma is a rare connective tissue disease that is manifested by cutaneous sclerosis
and variable systemic involvement. Two categories of scleroderma are known: systemic …

Morphea, also known as localized scleroderma, is a rare fibrosing disorder of the skin and
underlying tissues. Morphea is differentiated from systemic sclerosis based on the absence …

abstract Objectives To perform a systematic review of neurologic involvement in Systemic
sclerosis (SSc) and Localized Scleroderma (LS), describing clinical features, neuroimaging …

Parry-Romberg syndrome, also known as progressive hemifacial atrophy, is a rare disorder
characterized by unilateral facial atrophy affecting the skin, subcutaneous tissue, muscles …

Scleroderma comes from the Greek word for “hard skin” and refers to diseases associated
with excessive production of collagen resulting in fibrosis of skin and other affected organs …

Abstract Background Progressive Hemifacial Atrophy (PHA) is an acquired, typically
unilateral, facial distortion with unknown etiology. The true incidence of this disorder has not …

Scleroderma refers to a heterogeneous group of autoimmune fibrosing disorders. The
nomenclature of scleroderma has changed dramatically in recent years, with morphea …

Localized scleroderma (LS) is a complex disease characterized by a mixture of inflammation
and fibrosis of the skin that, especially in the pediatric population, also affects …

La livedo es una manifestación cutánea frecuente, que consiste en un eritema reticular de
origen vascular. Las dermatosis no vasculares con una disposición reticulada se reconocen …

We established diagnostic criteria and severity classification of localized scleroderma
because there is no established diagnostic criteria or widely accepted severity classification …