A Case of Congenital Cutis Laxa (Generalized Elastolysis)
نویسندگان
چکیده
منابع مشابه
Cutis laxa (elastolysis) in a patient with Sjögren's syndrome.
Cutis laxa (CL), or elastolysis, is a rare inherited or acquired connective tissue disorder where the skin becomes inelastic and hangs loosely in folds. Sjögren’s syndrome (SS) is a chronic inflammatory disease characterized by diminished lacrimal and salivary gland function. SS may be a primary disease and may accompany other rheumatologic diseases. To our knowledge, the simultaneous occurrenc...
متن کاملCutis laxa: case report.
Cutis laxa is a rare inherited or acquired disorder of elastic tissue characterized by inelastic and loose skin. Congenital cutis laxa may present with internal organ involvement, determining a worse prognosis. The authors present the case of a female patient with clinical manifestations suggestive of the hereditary form of the disease, with consanguineous parents (second-degree cousins) and a ...
متن کاملCongenital Cutis laxa associated with growth retardation.
Congenital cutis laxa is a rare, clinically and genetically heterogeneous group of inherited disorders. It is characterized by degenerative changes in elastic fibres and manifests with skin laxity. Here we presented a six-month old boy with congenital cutis laxa associated with growth retardation. We reveal ultrastructural findings and discussed the differential diagnosis.
متن کاملCutis Laxa syndrome: a case report
Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders characterized by a loose skin and variable systemic involvement (inguinal hernia, cardiopulmonary disease, and emphysema). Autosomal dominant, autosomal recessive and x-linked recessive patterns have been described in the inherited forms. Acquired forms of this disease have been associated with a prev...
متن کاملCongenital cutis laxa with retardation of growth and development.
Seven patients with congenital cutis laxa are presented. The associated features include developmental delay, joint laxity, wide anterior fontanelle, growth retardation, dental caries, and osteopenia. The heterogeneity and inheritance of congenital cutis laxa are discussed. This particular syndrome appears distinct and is likely to be autosomal recessive in view of the two brother-sister sib pa...
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ژورنال
عنوان ژورنال: Canadian Respiratory Journal
سال: 2005
ISSN: 1198-2241
DOI: 10.1155/2005/624875