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Alabaz D, Mungan N, Turgut M, Dalay C: Unusual Idiopathic Calcinosis Cutis Universalis in a Child.
Calcinosis cutis associated with SLE is dystrophic in nature and nearly always localised (calcinosis cutis circumscripta) but may infrequently occur as a generalised form referred to as calcinosis cutis universalis.
Vacuolar H+ATPase meets glycosylation in patients with cutis laxa.
Leukemia cutis manifests as cutaneous eruptions, which result from infiltration of leukemic cells into the skin.
unusual facies, deafness, bronzed hyperpigmentation of the skin, cutis laxa, mental retardation, and bony deformities) (4).
Lipoid proteinosis (LP), also known as hyalinosis cutis et mucosae, was first described by a Viennese dermatologist and otorhinolaryngologist, Urbach and Wiethe, in 1929 (1).
Propylthiouracil (PTU) has been the preferred therapy for Graves' disease during pregnancy, especially during first-trimester organogenesis, because methimazole (MMI) and carbimazole have been associated with aplasia cutis and rare embryopathy including choanal atresia, esophageal atresia, tracheoesophageal fistula, and athelia.
Lipoid proteinosis, which is also known in the literature as Urbach- Wiethe disease and hyalinosis cutis et mucosae, is a rare autosomal-recessive anomaly that primarily affects children.
We call this "goosebumps," but the medical name is cutis anserina.
Lipoid proteinosis (Urbach-Wiethe disease, hyalinosis cutis et mucosae) is an autosomal-recessive condition with variable penetrance.