{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,6,25]],"date-time":"2025-06-25T20:25:31Z","timestamp":1750883131313},"reference-count":27,"publisher":"Springer Science and Business Media LLC","issue":"10","license":[{"start":{"date-parts":[[2017,9,4]],"date-time":"2017-09-04T00:00:00Z","timestamp":1504483200000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Hautarzt"],"published-print":{"date-parts":[[2017,10]]},"DOI":"10.1007\/s00105-017-4035-z","type":"journal-article","created":{"date-parts":[[2017,9,4]],"date-time":"2017-09-04T05:19:14Z","timestamp":1504502354000},"page":"796-802","update-policy":"http:\/\/dx.doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Das rote, schuppende Baby: ein kinderdermatologischer Notfall"],"prefix":"10.1007","volume":"68","author":[{"given":"H.","family":"Ott","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"Grothaus","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2017,9,4]]},"reference":[{"issue":"12","key":"4035_CR1","doi-asserted-by":"publisher","first-page":"1070","DOI":"10.1111\/j.1610-0387.2008.06891.x","volume":"6","author":"H Ott","year":"2008","unstructured":"Ott H, H\u00fctten M, Baron JM et\u00a0al (2008) Neonatal and infantile erythrodermas. J\u00a0Dtsch Dermatol Ges 6(12):1070\u20131085","journal-title":"J Dtsch Dermatol Ges"},{"issue":"4","key":"4035_CR2","doi-asserted-by":"publisher","first-page":"236","DOI":"10.1007\/s00105-015-3610-4","volume":"66","author":"H Ott","year":"2015","unstructured":"Ott H, Guthmann F, Ludwikowski B (2015) Interdisciplinary care of newborns with epidermolysis bullosa and severe congenital ichthyoses. Hautarzt 66(4):236\u2013244","journal-title":"Hautarzt"},{"issue":"5","key":"4035_CR3","doi-asserted-by":"publisher","first-page":"302","DOI":"10.1111\/j.1346-8138.2007.00277.x","volume":"34","author":"MA Al-Dhalimi","year":"2007","unstructured":"Al-Dhalimi MA (2007) Neonatal and infantile erythroderma: a\u00a0clinical and follow-up study of 42 cases. J\u00a0Dermatol 34(5):302\u2013307","journal-title":"J Dermatol"},{"issue":"4","key":"4035_CR4","doi-asserted-by":"publisher","first-page":"438","DOI":"10.1097\/MOP.0b013e32833bc396","volume":"22","author":"S Fraitag","year":"2010","unstructured":"Fraitag S, Bodemer C (2010) Neonatal erythroderma. Curr Opin Pediatr 22(4):438\u2013444","journal-title":"Curr Opin Pediatr"},{"issue":"7","key":"4035_CR5","doi-asserted-by":"publisher","first-page":"875","DOI":"10.1001\/archderm.136.7.875","volume":"136","author":"A Pruszkowski","year":"2000","unstructured":"Pruszkowski A, Bodemer C, Fraitag S et\u00a0al (2000) Neonatal and infantile erythrodermas: a\u00a0retrospective study of 51 patients. Arch Dermatol 136(7):875\u2013880","journal-title":"Arch Dermatol"},{"issue":"3","key":"4035_CR6","doi-asserted-by":"publisher","first-page":"318","DOI":"10.1001\/archderm.139.3.318","volume":"139","author":"P Foley","year":"2003","unstructured":"Foley P, Zuo Y, Plunkett A et al (2003) The frequency of common skin conditions in preschool-aged children in Australia: seborrheic dermatitis and pityriasis capitis (cradle cap). Arch Dermatol 139(3):318\u2013322","journal-title":"Arch Dermatol"},{"issue":"4","key":"4035_CR7","doi-asserted-by":"publisher","first-page":"359","DOI":"10.1111\/pai.12388","volume":"26","author":"E Draaisma","year":"2015","unstructured":"Draaisma E, Garcia-Marcos L, Mallol J et al (2015) A multinational study to compare prevalence of atopic dermatitis in the first year of life. Pediatr Allergy Immunol 26(4):359\u2013366","journal-title":"Pediatr Allergy Immunol"},{"issue":"Suppl 1","key":"4035_CR8","doi-asserted-by":"publisher","first-page":"2","DOI":"10.1111\/bjd.12933","volume":"170","author":"M Deleuran","year":"2014","unstructured":"Deleuran M, Vestergaard C (2014) Clinical heterogeneity and differential diagnosis of atopic dermatitis. Br J Dermatol 170(Suppl 1):2\u20136","journal-title":"Br J Dermatol"},{"issue":"6","key":"4035_CR9","doi-asserted-by":"publisher","first-page":"1242","DOI":"10.1111\/bjd.14507","volume":"174","author":"E Burden-Teh","year":"2016","unstructured":"Burden-Teh E, Thomas KS, Ratib S et al (2016) The epidemiology of childhood psoriasis: a\u00a0scoping review. Br J Dermatol 174(6):1242\u20131257","journal-title":"Br J Dermatol"},{"issue":"2","key":"4035_CR10","doi-asserted-by":"publisher","first-page":"249","DOI":"10.1111\/j.1600-0560.2009.01344.x","volume":"37","author":"S Leclerc-Mercier","year":"2010","unstructured":"Leclerc-Mercier S, Bodemer C, Bourdon-Lanoy E et al (2010) Early skin biopsy is helpful for the diagnosis and management of neonatal and infantile erythrodermas. J\u00a0Cutan Pathol 37(2):249\u2013255","journal-title":"J Cutan Pathol"},{"issue":"3","key":"4035_CR11","doi-asserted-by":"publisher","first-page":"332","DOI":"10.1111\/j.1525-1470.2008.00676.x","volume":"25","author":"JS Lehman","year":"2008","unstructured":"Lehman JS, Rahil AK (2008) Congenital psoriasis: case report and literature review. Pediatr Dermatol 25(3):332\u2013338","journal-title":"Pediatr Dermatol"},{"issue":"4","key":"4035_CR12","doi-asserted-by":"publisher","first-page":"349","DOI":"10.1111\/j.1525-1470.2010.01084.x","volume":"27","author":"ST Oliveira de","year":"2010","unstructured":"de Oliveira ST, Maragno L, Arnone M et\u00a0al (2010) Generalized pustular psoriasis in childhood. Pediatr Dermatol 27(4):349\u2013354","journal-title":"Pediatr Dermatol"},{"issue":"1","key":"4035_CR13","doi-asserted-by":"publisher","first-page":"163","DOI":"10.1016\/j.ajhg.2012.05.010","volume":"91","author":"D Fuchs-Telem","year":"2012","unstructured":"Fuchs-Telem D, Sarig O, van Steensel MA et al (2012) Familial pityriasis rubra pilaris is caused by mutations in CARD14. Am J Hum Genet 91(1):163\u2013170","journal-title":"Am J Hum Genet"},{"issue":"3","key":"4035_CR14","doi-asserted-by":"publisher","first-page":"242","DOI":"10.1111\/1346-8138.13243","volume":"43","author":"T Takeichi","year":"2016","unstructured":"Takeichi T, Akiyama M (2016) Inherited ichthyosis: Non-syndromic forms. J\u00a0Dermatol 43(3):242\u2013251","journal-title":"J Dermatol"},{"issue":"6","key":"4035_CR15","doi-asserted-by":"publisher","first-page":"1362","DOI":"10.1016\/j.jaad.2012.05.036","volume":"67","author":"R Prado","year":"2012","unstructured":"Prado R, Ellis LZ, Gamble R et\u00a0al (2012) Collodion baby: an update with a\u00a0focus on practical management. J\u00a0Am Acad Dermatol 67(6):1362\u20131374","journal-title":"J Am Acad Dermatol"},{"issue":"4","key":"4035_CR16","doi-asserted-by":"publisher","first-page":"473","DOI":"10.2340\/00015555-2299","volume":"96","author":"A Hotz","year":"2016","unstructured":"Hotz A, Oji V, Bourrat E et\u00a0al (2016) Expanding the clinical and genetic spectrum of KRT1, KRT2 and KRT10 mutations in Keratinopathic Ichthyosis. Acta Derm Venereol 96(4):473\u2013478","journal-title":"Acta Derm Venereol"},{"issue":"1","key":"4035_CR17","doi-asserted-by":"publisher","first-page":"19","DOI":"10.1891\/0730-0832.35.1.19","volume":"35","author":"M Avril","year":"2016","unstructured":"Avril M, Riley C (2016) Management of Epidermolytic Ichthyosis in the newborn. Neonatal Netw 35(1):19\u201328","journal-title":"Neonatal Netw"},{"issue":"4","key":"4035_CR18","doi-asserted-by":"publisher","first-page":"238","DOI":"10.1016\/j.ejmg.2015.01.011","volume":"58","author":"BG Nur","year":"2015","unstructured":"Nur BG, Gencpinar P, Yuzbas\u0131oglu A et al (2015) Chanarin-Dorfman syndrome: genotype-phenotype correlation. Eur J Med Genet 58(4):238\u2013242","journal-title":"Eur J Med Genet"},{"issue":"4","key":"4035_CR19","doi-asserted-by":"publisher","first-page":"830","DOI":"10.1111\/j.1365-2133.2011.10756.x","volume":"166","author":"J Ca\u00f1ueto","year":"2012","unstructured":"Ca\u00f1ueto J, Gir\u00f3s M, Ciria S et al (2012) Clinical, molecular and biochemical characterization of nine Spanish families with Conradi-H\u00fcnermann-Happle syndrome: new insights into X\u2011linked dominantchondrodysplasia punctata with a\u00a0comprehensive review of the literature. Br J Dermatol 166(4):830\u2013838","journal-title":"Br J Dermatol"},{"issue":"1","key":"4035_CR20","doi-asserted-by":"publisher","first-page":"e1","DOI":"10.1212\/WNL.0000000000003456","volume":"88","author":"M Nagappa","year":"2017","unstructured":"Nagappa M, Bindu PS, Chiplunkar S et al (2017) Child Neurology: Sj\u00f6gren-Larsson syndrome. Neurology 88(1):e1\u2013e4","journal-title":"Neurology"},{"issue":"4","key":"4035_CR21","doi-asserted-by":"publisher","first-page":"435","DOI":"10.1001\/jamadermatol.2015.5827","volume":"152","author":"K Hannula-Jouppi","year":"2016","unstructured":"Hannula-Jouppi K, Laasanen SL, Ilander M et al (2016) Intrafamily and Interfamilial phenotype variation and immature immunity in patients with Netherton syndrome and Finnish SPINK5 founder mutation. JAMA Dermatol 152(4):435\u2013442","journal-title":"JAMA Dermatol"},{"issue":"2","key":"4035_CR22","doi-asserted-by":"publisher","first-page":"274","DOI":"10.1016\/j.ajhg.2010.07.005","volume":"87","author":"V Oji","year":"2010","unstructured":"Oji V, Eckl KM, Aufenvenne K et\u00a0al (2010) Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease. Am J Hum Genet 87(2):274\u2013281","journal-title":"Am J Hum Genet"},{"issue":"4","key":"4035_CR23","doi-asserted-by":"publisher","first-page":"808","DOI":"10.1016\/j.jaci.2014.07.061","volume":"134","author":"L Samuelov","year":"2014","unstructured":"Samuelov L, Sprecher E (2014) Peeling off the genetics of atopic dermatitis-like congenital disorders. J\u00a0Allergy Clin Immunol 134(4):808\u2013815","journal-title":"J Allergy Clin Immunol"},{"key":"4035_CR24","doi-asserted-by":"publisher","first-page":"209","DOI":"10.1016\/j.jaci.2009.10.023","volume":"125","author":"B Cassani","year":"2010","unstructured":"Cassani B, Poliani PL, Moratto D et\u00a0al (2010) Defect of regulatory T cells in patients with Omenn syndrome. J\u00a0Allergy Clin Immunol 125:209\u2013216","journal-title":"J Allergy Clin Immunol"},{"issue":"2","key":"4035_CR25","doi-asserted-by":"publisher","first-page":"497","DOI":"10.1007\/s12026-015-8723-4","volume":"64","author":"X Bai","year":"2016","unstructured":"Bai X, Liu J, Zhang Z et\u00a0al (2016) Clinical, immunologic, and genetic characteristics of RAG mutations in 15 Chinese patients with SCID and Omenn syndrome. Immunol Res 64(2):497\u2013507","journal-title":"Immunol Res"},{"key":"4035_CR26","doi-asserted-by":"publisher","first-page":"410","DOI":"10.1111\/j.1365-2230.2008.02940.x","volume":"34","author":"S Minakawa","year":"2009","unstructured":"Minakawa S, Nakano H, Takeda H et\u00a0al (2009) Chromosome 22q11.2 deletion syndrome associated with severe eczema. Clin Exp Dermatol 34:410\u2013411","journal-title":"Clin Exp Dermatol"},{"issue":"2","key":"4035_CR27","doi-asserted-by":"publisher","first-page":"628","DOI":"10.1016\/j.jaci.2016.04.049","volume":"139","author":"J Wahlstrom","year":"2017","unstructured":"Wahlstrom J, Patel K, Eckhert E et al (2017) Transplacental maternal engraftment and posttransplantation graft-versus-host disease in children with severe combined immunodeficiency. J\u00a0Allergy Clin Immunol 139(2):628\u2013633","journal-title":"J Allergy Clin Immunol"}],"container-title":["Der Hautarzt"],"original-title":[],"language":"de","link":[{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00105-017-4035-z\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00105-017-4035-z.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00105-017-4035-z.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2018,9,11]],"date-time":"2018-09-11T16:58:35Z","timestamp":1536685115000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00105-017-4035-z"}},"subtitle":["Klinik und Differenzialdiagnosen neonataler Erythrodermien"],"short-title":[],"issued":{"date-parts":[[2017,9,4]]},"references-count":27,"journal-issue":{"issue":"10","published-print":{"date-parts":[[2017,10]]}},"alternative-id":["4035"],"URL":"https:\/\/doi.org\/10.1007\/s00105-017-4035-z","relation":{},"ISSN":["0017-8470","1432-1173"],"issn-type":[{"value":"0017-8470","type":"print"},{"value":"1432-1173","type":"electronic"}],"subject":[],"published":{"date-parts":[[2017,9,4]]}}}