Introduction: Morphea is a rare fibrosing disorder of the skin and underlying tissues. Deep morphea involves the deep dermis, subcutis, fascia, muscle, and bone. The above structures may be involved independently or in combination. Case report: We describe a case of deep morphea presenting as muscle weakness, independent of skin lesions, in a child with generalized morphea. Discussion: Muscle weakness, even in the absence of overlying or progressive skin sclerosis, can be deep morphea, especially when segmental and associated with atrophy
Disabling Pansclerotic Morphea (DPM) is a rare fibrotic skin disorder that is characterized by rapid...
SUMMARY An 18 year old girl concurrently developed skin lesions of morphoea (localised scleroderma) ...
Dystrophinopathy is caused by mutations in the dystrophin gene at Xp21. Although manifesting carrier...
Contains fulltext : 70571.pdf (publisher's version ) (Closed access)Localized scle...
The objective to describe a rare case of morphea disease, it is an autoimmune disease in which an el...
Morphea is a variant of localized scleroderma in which lesions are usually limited to the skin and s...
Etiologies for childhood-onset diffuse joint contractures encompass a large group of inherited disor...
ceral involvement (kidneys, lungs, digestive tract, heart) so the disease can be fatal (progressive ...
Localized scleroderma (also called morphea) is a term encompassing a spectrum of sclerotic autoimmun...
Supplemental figure 1. Clinical variants of morphea: (A) plaque type on the upper back (B) linear (e...
Localized scleroderma, also known as morphea, is a rare condition characterized by progressive scler...
Generalized morphea is a subtype of localized scleroderma, which lacks systemic manifestations and d...
AbstractIntroductionHarlequin ichthyosis (HI) is a severe and rare hereditary congenital skin disord...
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, p...
A 12 year old boy presented with pain and stiffness in large joints with tautness of skin, dysphagia...
Disabling Pansclerotic Morphea (DPM) is a rare fibrotic skin disorder that is characterized by rapid...
SUMMARY An 18 year old girl concurrently developed skin lesions of morphoea (localised scleroderma) ...
Dystrophinopathy is caused by mutations in the dystrophin gene at Xp21. Although manifesting carrier...
Contains fulltext : 70571.pdf (publisher's version ) (Closed access)Localized scle...
The objective to describe a rare case of morphea disease, it is an autoimmune disease in which an el...
Morphea is a variant of localized scleroderma in which lesions are usually limited to the skin and s...
Etiologies for childhood-onset diffuse joint contractures encompass a large group of inherited disor...
ceral involvement (kidneys, lungs, digestive tract, heart) so the disease can be fatal (progressive ...
Localized scleroderma (also called morphea) is a term encompassing a spectrum of sclerotic autoimmun...
Supplemental figure 1. Clinical variants of morphea: (A) plaque type on the upper back (B) linear (e...
Localized scleroderma, also known as morphea, is a rare condition characterized by progressive scler...
Generalized morphea is a subtype of localized scleroderma, which lacks systemic manifestations and d...
AbstractIntroductionHarlequin ichthyosis (HI) is a severe and rare hereditary congenital skin disord...
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, p...
A 12 year old boy presented with pain and stiffness in large joints with tautness of skin, dysphagia...
Disabling Pansclerotic Morphea (DPM) is a rare fibrotic skin disorder that is characterized by rapid...
SUMMARY An 18 year old girl concurrently developed skin lesions of morphoea (localised scleroderma) ...
Dystrophinopathy is caused by mutations in the dystrophin gene at Xp21. Although manifesting carrier...