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Article

Netherton syndrome: report of identical twins presenting with severe atopic dermatitis.

European journal of pediatrics - 1 Sept 2006

Kilic Gurkan, Guler Nermin, Ones Ulker, Tamay Zeynep, Guzel Pinar

Abstract excerpt

We report the cases of 4-year-old identical twin sisters who presented with severe atopic dermatitis with intractable skin manifestations and multiple food allergies. Netherton syndrome (NS) (OMIM 256500) was suspected due to very high serum IgE levels, growth retardation, severe food allergies a...

Read the complete abstract on PubMed

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Share to Dermatitis, Atopic
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Share to Ichthyosiform Erythroderma, Congenital

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Proteinase Inhibitory Proteins, Secretory

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Share to Serine Peptidase Inhibitor Kazal-Type 5

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Source

Identifiers

PMID: 16670861
DOI: 10.1007/s00431-006-0141-0

Genes

SPINK5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16670861-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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Netherton syndrome: report of identical twins presenting with severe atopic dermatitis.PMID 16670861Read ↗

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Netherton syndrome and its multifaceted defective protein LEKTI.Semantic proximity Read ↗

Netherton syndrome: A neonatal case with respiratory insufficiency.Semantic proximity Read ↗

Netherton Syndrome -- a therapeutic challenge in childhoodSemantic proximity Read ↗

Netherton Syndrome Caused by Heterozygous Frameshift Mutation Combined with Homozygous c.1258A>G Polymorphism in SPINK5 Gene.Semantic proximity Read ↗

A novel SPINK5 mutation and successful subcutaneous immunoglobulin replacement therapy in a child with Netherton syndrome.Semantic proximity Read ↗

Netherton syndrome: report of two Taiwanese siblings with staphylococcal scalded skin syndrome and mutation of SPINK5.Semantic proximity Read ↗

The challenging management of a series of 43 infants with Netherton syndrome: unexpected complications and novel mutations.Semantic proximity Read ↗

Netherton Syndrome in a Mother and Her Two Children.Semantic proximity Read ↗

A Novel SPINK5 Gene Mutation Associated with Netherton Syndrome in an Omani Patient.Semantic proximity Read ↗

Intrafamily and Interfamilial Phenotype Variation and Immature Immunity in Patients With Netherton Syndrome and Finnish SPINK5 Founder Mutation.Semantic proximity Read ↗

A compound heterozygous mutation of the SPINK5 gene in a Taiwanese boy with Netherton syndrome.Semantic proximity Read ↗

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