Developmental retardation in postinflammatory elastolysis and cutis laxa
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 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 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...
متن کاملDiscriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica
Cutis laxa is a heterogeneous condition characterized by redundant, sagging, inelastic, and wrinkled skin. The inherited forms of this disease are rare and can have autosomal dominant, autosomal recessive, or X-linked inheritance. Three of the autosomal recessive cutis laxa syndromes, namely cutis laxa IIA (ARCL2A), cutis laxa IIB (ARCL2B), and geroderma osteodysplastica (GO), have very similar...
متن کاملSotos syndrome and cutis laxa.
Characteristics suggestive of connective tissue dysfunction have been described in Sotos syndrome and include joint hyperextensibility, pes planus, and a high arched palate. A variety of cutis laxa syndromes have also been described, some of them exhibiting mental retardation, but no reports have drawn an association with overgrowth or abnormal facies characteristic of Sotos syndrome. We report...
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ژورنال
عنوان ژورنال: Indian Journal of Dermatology, Venereology, and Leprology
سال: 2016
ISSN: 0378-6323
DOI: 10.4103/0378-6323.164212