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. "Cutis Laxa Congénita Aociada con Retardo del Crecimiento" RESUMEN El laxa del cutis es un grupo raro, clínica y genéticamente heterogéneo de desórdenes heredados. Esta afección se caracteriza por cambios degenerativos en las fibras elásticas y se manifiesta en la hiperlaxitud de la piel. Aquí presentamos el caso de un niño de seis meses con cutis laxa congénita asoc...
Autosomal recessive cutis laxa is a genetically heterogeneous condition. Its molecular basis is larg...
Autosomal recessive cutis laxa is a genetically heterogeneous condition. Its molecular basis is larg...
Congenital cutis laxa is a genetically heterogeneous condition presenting with loose and redundant s...
The Cutis laxa syndrome is a group of rare heterogeneous disorders of the elastic tissue characteriz...
Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders chara...
Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders chara...
Cutis laxa is a connective tissue disorder caused by deficiency of fibro elastic plexus, which can i...
Cutis laxa is a rare disorder characterized by degenerative changes in elastic fibres. Congenital c...
Cutis laxa is a rare disorder characterized by degenerative changes in elastic fibres. Congenital c...
Cutis laxa is a rare skin disorder, characterized by redundant, inelastic and with an appearance of ...
Cutis laxa is a rare disorder characterized by degenerative changes in elastic fibres. Congenital cu...
Cutis laxa is an inherited or acquired disease characterized by redundant, sagging and inelastic ski...
Cutis laxa (CL) is a rare congenital and acquired disorder characterized by loose and redundant skin...
Cutis laxa (CL) is a rare connective tissue disorder characterized by loose, sagging, and redundant ...
La cutis laxa es un trastorno infrecuente de la piel, que se caracteriza por ser redundante, inelást...
Autosomal recessive cutis laxa is a genetically heterogeneous condition. Its molecular basis is larg...
Autosomal recessive cutis laxa is a genetically heterogeneous condition. Its molecular basis is larg...
Congenital cutis laxa is a genetically heterogeneous condition presenting with loose and redundant s...
The Cutis laxa syndrome is a group of rare heterogeneous disorders of the elastic tissue characteriz...
Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders chara...
Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders chara...
Cutis laxa is a connective tissue disorder caused by deficiency of fibro elastic plexus, which can i...
Cutis laxa is a rare disorder characterized by degenerative changes in elastic fibres. Congenital c...
Cutis laxa is a rare disorder characterized by degenerative changes in elastic fibres. Congenital c...
Cutis laxa is a rare skin disorder, characterized by redundant, inelastic and with an appearance of ...
Cutis laxa is a rare disorder characterized by degenerative changes in elastic fibres. Congenital cu...
Cutis laxa is an inherited or acquired disease characterized by redundant, sagging and inelastic ski...
Cutis laxa (CL) is a rare congenital and acquired disorder characterized by loose and redundant skin...
Cutis laxa (CL) is a rare connective tissue disorder characterized by loose, sagging, and redundant ...
La cutis laxa es un trastorno infrecuente de la piel, que se caracteriza por ser redundante, inelást...
Autosomal recessive cutis laxa is a genetically heterogeneous condition. Its molecular basis is larg...
Autosomal recessive cutis laxa is a genetically heterogeneous condition. Its molecular basis is larg...
Congenital cutis laxa is a genetically heterogeneous condition presenting with loose and redundant s...