Typical features of Netherton syndrome are congenital ichthyosiform erythroderma, atopic diathesis and trichorrhexis nodosa. Here in this report, we present a case with congenital ichthyosis with atopy presenting later. We wanted to discuss the importance of whole exome sequencing to diagnose the atypical presentations of common syndromes
Netherton syndrome (NS, OMIM #256500) is a rare autosomal recessive disease characterized by a triad...
© 2017 by the American Academy of Dermatology, Inc. Published by Elsevier, Inc. This is an open acce...
Netherton syndrome is a severe, autosomal recessive form of ichthyosis associated with mutations in ...
WOS: 000436882600013Typical features of Netherton syndrome are congenital ichthyosiform erythroderma...
Netherton syndrome (NS) is a rare autosomal recessive disorder characterized by a triad of congenita...
Introduction. Comèl-Netherton syndrome is a rare autosomal recessive genodermatosis characterized b...
Ichthyosis linearis circumflexa (ILC) presents as serpiginous and migratory erythematous patches wit...
Introduction: Ichthyosis vulgaris is a common disorder characterized clinically by xerosis, excessiv...
Netherton syndrome is a severe, autosomal recessive form of ichthyosis associated with mutations in ...
Netherton syndrome is a severe autosomal recessive skin disorder characterized by congenital erythro...
Netherton syndrome is a rare, multisystem, autosomal recessive genodermatosis characterized by a tri...
Comèl-Netherton syndrome (OMIM 256500) is an autosomal recessive, hereditary disease, independently ...
Copyright © 2015 Chatziioannidis Ilias et al. This is an open access article distributed under the C...
Netherton syndrome (NS [MIM 256500]) is a rare and severe autosomal recessive disorder characterized...
Netherton syndrome is a rare autosomal recessive disorder associated with mutation of the SPINK5 gen...
Netherton syndrome (NS, OMIM #256500) is a rare autosomal recessive disease characterized by a triad...
© 2017 by the American Academy of Dermatology, Inc. Published by Elsevier, Inc. This is an open acce...
Netherton syndrome is a severe, autosomal recessive form of ichthyosis associated with mutations in ...
WOS: 000436882600013Typical features of Netherton syndrome are congenital ichthyosiform erythroderma...
Netherton syndrome (NS) is a rare autosomal recessive disorder characterized by a triad of congenita...
Introduction. Comèl-Netherton syndrome is a rare autosomal recessive genodermatosis characterized b...
Ichthyosis linearis circumflexa (ILC) presents as serpiginous and migratory erythematous patches wit...
Introduction: Ichthyosis vulgaris is a common disorder characterized clinically by xerosis, excessiv...
Netherton syndrome is a severe, autosomal recessive form of ichthyosis associated with mutations in ...
Netherton syndrome is a severe autosomal recessive skin disorder characterized by congenital erythro...
Netherton syndrome is a rare, multisystem, autosomal recessive genodermatosis characterized by a tri...
Comèl-Netherton syndrome (OMIM 256500) is an autosomal recessive, hereditary disease, independently ...
Copyright © 2015 Chatziioannidis Ilias et al. This is an open access article distributed under the C...
Netherton syndrome (NS [MIM 256500]) is a rare and severe autosomal recessive disorder characterized...
Netherton syndrome is a rare autosomal recessive disorder associated with mutation of the SPINK5 gen...
Netherton syndrome (NS, OMIM #256500) is a rare autosomal recessive disease characterized by a triad...
© 2017 by the American Academy of Dermatology, Inc. Published by Elsevier, Inc. This is an open acce...
Netherton syndrome is a severe, autosomal recessive form of ichthyosis associated with mutations in ...