Morphea, also known as localized scleroderma, encompasses a group of idiopathic sclerotic
skin diseases. The spectrum ranges from relatively mild phenotypes, which generally cause …

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

In 2012, a European initiative called Single Hub and Access point for paediatric
Rheumatology in Europe (SHARE) was launched to optimise and disseminate diagnostic …

Localized scleroderma designates a heterogeneous group of sclerotic skin disorders.
Depending on the subtype, severity, and site affected, adjacent structures such as adipose …

Morphea, also known as localized scleroderma, is a chronic inflammatory connective tissue
disorder with variable clinical presentations, that affects both adults and children. It is …

Morphea is a rare autoimmune condition causing inflammation and sclerosis of the skin and
underlying soft tissue. It is characterized by periods of activity (inflammation admixed with …

Parry Romberg syndrome is a rare progressive hemiatrophy of the face that typically occurs
in children and young adults and has a peculiar progression that ceases without apparent …

Abstract Introduction Parry–Romberg syndrome (PRS) and en coup de sabre (ECS) are
variants of morphea. Although numerous findings on central nervous system (CNS) imaging …

Background Localized scleroderma is a rare inflammatory skin disorder that affects the skin
and sometimes underlying subcutaneous tissue, muscles or bones. The disease has two …

Background Localized scleroderma, known as morphea, is a connective tissue disorder
characterized by inflammation and fibrosis of the skin and the soft tissue. There exist no …