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3. Erythroderma in a newborn infant suggesting Omenn syndrome. Ren F; Bai X; Elston DM Br J Dermatol; 2020 Sep; 183(3):e63. PubMed ID: 32399979 [No Abstract] [Full Text] [Related]
4. An erythematous rash, diarrhea, failure to thrive, and lymphadenopathy in a 3-month-old girl. Sicherer SH; Lederman HM Ann Allergy Asthma Immunol; 1997 Mar; 78(3):253-8. PubMed ID: 9087148 [No Abstract] [Full Text] [Related]
5. [Neonatal erythrodermia - early manifestation of Omenn's syndrome]. Wozniakowska-Gesicka T; Wisniewska-Ligier M; Borowska-Rybus B Med Wieku Rozwoj; 2002; 6(1):23-9. PubMed ID: 12177510 [TBL] [Abstract][Full Text] [Related]
6. Unusual dermatological presentation and immune phenotype in SCID due to an IL7R mutation: the value of whole-exome sequencing and the potential benefit of newborn screening. Marquardt L; Lacour M; Hoernes M; Opitz L; Lecca R; Volkmer B; Reichenbach J; Hohl D; Ansari M; Ozsahin H; Güngör T; Pachlopnik Schmid J J Eur Acad Dermatol Venereol; 2017 Mar; 31(3):e147-e148. PubMed ID: 27593400 [No Abstract] [Full Text] [Related]
8. A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome. Chou J; Hanna-Wakim R; Tirosh I; Kane J; Fraulino D; Lee YN; Ghanem S; Mahfouz I; Mégarbané A; Lefranc G; Inati A; Dbaibo G; Giliani S; Notarangelo LD; Geha RS; Massaad MJ J Allergy Clin Immunol; 2012 Dec; 130(6):1414-6. PubMed ID: 22841008 [No Abstract] [Full Text] [Related]
9. In utero acute graft-versus-host disease in a neonate with severe combined immunodeficiency. Alain G; Carrier C; Beaumier L; Bernard J; Lemay M; Lavoie A J Am Acad Dermatol; 1993 Nov; 29(5 Pt 2):862-5. PubMed ID: 8408828 [TBL] [Abstract][Full Text] [Related]
10. Exfoliative erythroderma, recurrent infections, generalized lymphadenopathy and hepatosplenomegaly in a newborn: Omenn syndrome. Tatli MM; Sarraoglu S; Shermatov K; Gurel MS; Karadag A Australas J Dermatol; 2007 May; 48(2):133-4. PubMed ID: 17535207 [No Abstract] [Full Text] [Related]
12. Diffuse Erythematous Rash in a Child: A Journey to Diagnosis. Hogan JC; Keifer A; Murphy AE; Beeman G; Hysmith N Clin Pediatr (Phila); 2020 Jun; 59(7):730-735. PubMed ID: 32075425 [No Abstract] [Full Text] [Related]
13. Proposal of Slovenian guidelines for the diagnosis of neonatal erythroderma with a case report of Omenn syndrome. Starbek Zorko M; Štublar Krašovec A; Dragoš V Acta Dermatovenerol Alp Pannonica Adriat; 2023 Jun; 32(2):57-61. PubMed ID: 37365893 [TBL] [Abstract][Full Text] [Related]
14. Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: a case of Omenn syndrome. Cuperus E; Montfrans JMV; Gijn MEV; Bastiaens MT; Willigen MM; Leguit RJ; Brijnzeel-Koomen CA; RusseL IM; Pasmans SG Eur J Dermatol; 2017 Jun; 27(3):313-314. PubMed ID: 28414192 [No Abstract] [Full Text] [Related]
15. [Ichtyosiform erythroderma revealing a severe combined immunodeficiency]. Ghariani Fetoui N; Boussofara L; Hmida D; Mokni S; Mekki N; Ben Mustapha I; Belajouza C; Ghariani N; Picard C; Denguezli M Ann Dermatol Venereol; 2020 Feb; 147(2):131-134. PubMed ID: 31973905 [TBL] [Abstract][Full Text] [Related]
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17. [Facets of scaly erythema. Morphologically and descriptively oriented dermatological diagnosis (6)]. Schulz H MMW Fortschr Med; 1999 Oct; 141(41):39-44. PubMed ID: 10904636 [No Abstract] [Full Text] [Related]