Literature DB >> 16670861

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

Gurkan Kilic1, Nermin Guler, Ulker Ones, Zeynep Tamay, Pinar Guzel.   

Abstract

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 and typical hair finding (trichorrhexis invaginata). A definite diagnosis was made by genetic analysis. Our cases are unique in being the first identical twins with NS diagnosed by a novel mutation in the SPINK5 gene. NS should be considered in differential diagnosis in children who have generalized erythema with intractable eczematous lesions and elevated levels of IgE.

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Year:  2006        PMID: 16670861     DOI: 10.1007/s00431-006-0141-0

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  25 in total

1.  Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping.

Authors:  S Chavanas; C Garner; C Bodemer; M Ali; D H Teillac; J Wilkinson; J L Bonafé; M Paradisi; D P Kelsell; S i Ansai; Y Mitsuhashi; M Larrègue; I M Leigh; J I Harper; A Taïeb; Y d Prost; L R Cardon; A Hovnanian
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

2.  SPINK5: a gene for atopic dermatitis and asthma.

Authors:  M F Moffatt
Journal:  Clin Exp Allergy       Date:  2004-03       Impact factor: 5.018

3.  Generalized exfoliative erythroderma since birth. Netherton syndrome.

Authors:  Laila El Shabrawi-Caelen; Josef Smolle; Dieter Metze; Gabriele Ginter-Hanselmayer; Michael Raghunath; Heiko Traupe; Helmut Kerl
Journal:  Arch Dermatol       Date:  2004-10

4.  [Not Available].

Authors:  M COMEL
Journal:  Dermatologica       Date:  1949

Review 5.  Neonatal erythroderma: differential diagnosis and management of the "red baby".

Authors:  P H Hoeger; J I Harper
Journal:  Arch Dis Child       Date:  1998-08       Impact factor: 3.791

6.  Netherton syndrome presenting as congenital psoriasis.

Authors:  T Shwayder; S Banerjee
Journal:  Pediatr Dermatol       Date:  1997 Nov-Dec       Impact factor: 1.588

7.  Significant absorption of topical tacrolimus in 3 patients with Netherton syndrome.

Authors:  A Allen; E Siegfried; R Silverman; M L Williams; P M Elias; S K Szabo; N J Korman
Journal:  Arch Dermatol       Date:  2001-06

8.  Severe hypernatremic dehydration in an infant with Netherton syndrome.

Authors:  C Stoll; Y Alembik; D Tchomakov; J Messer; E Heid; N Boehm; P Calvas; A Hovnanian
Journal:  Genet Couns       Date:  2001

Review 9.  Tay or IBIDS syndrome. A case with growth and mental retardation, congenital ichthyosis and brittle hair.

Authors:  H K Blomquist; O Bäck; M Fagerlund; G Holmgren; C Stecksén-Blicks
Journal:  Acta Paediatr Scand       Date:  1991-12

10.  Successful treatment of Netherton's syndrome with topical calcipotriol.

Authors:  Aleksandar Godic; Vlasta Dragos
Journal:  Eur J Dermatol       Date:  2004 Mar-Apr       Impact factor: 3.328

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  5 in total

Review 1.  Netherton Syndrome: A Genotype-Phenotype Review.

Authors:  Constantina A Sarri; Angeliki Roussaki-Schulze; Yiannis Vasilopoulos; Efterpi Zafiriou; Aikaterini Patsatsi; Costas Stamatis; Polyxeni Gidarokosta; Dimitrios Sotiriadis; Theologia Sarafidou; Zissis Mamuris
Journal:  Mol Diagn Ther       Date:  2017-04       Impact factor: 4.074

2.  A novel SPINK5 donor splice site variant in a child with Netherton syndrome.

Authors:  Dillon Mintoff; Isabella Borg; Julia Vornweg; Liam Mercieca; Rijad Merdzanic; Johannes Numrich; Susan Aquilina; Nikolai Paul Pace; Judith Fischer
Journal:  Mol Genet Genomic Med       Date:  2021-02-03       Impact factor: 2.183

3.  Netherton syndrome caused by compound heterozygous mutation, c.80A>G mutation in SPINK5 and large-sized genomic deletion mutation, and successful treatment of intravenous immunoglobulin.

Authors:  Zhen Zhang; Chaolan Pan; Ruoqu Wei; Huaguo Li; Yijun Yang; Jiawen Chen; Ming Li; Zhirong Yao
Journal:  Mol Genet Genomic Med       Date:  2021-01-16       Impact factor: 2.183

Review 4.  Netherton Syndrome in Children: Management and Future Perspectives.

Authors:  Federica Barbati; Mattia Giovannini; Teresa Oranges; Lorenzo Lodi; Simona Barni; Elio Novembre; Ermanno Baldo; Mario Cristofolini; Stefano Stagi; Silvia Ricci; Francesca Mori; Cesare Filippeschi; Chiara Azzari; Giuseppe Indolfi
Journal:  Front Pediatr       Date:  2021-05-10       Impact factor: 3.418

5.  Netherton Syndrome: A Case Report and Review of Literature.

Authors:  Hafiz M Kashif Saleem; Muhammad Faizan Shahid; Amir Shahbaz; Atif Sohail; Muhammad Arslan Shahid; Issac Sachmechi
Journal:  Cureus       Date:  2018-07-30
  5 in total

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