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Literature DB >> 27886899

Atopic Dermatitis and Allergic Urticaria: Cutaneous Manifestations of Immunodeficiency.

Martin Robert Gaudinski¹, Joshua D Milner².

Abstract

Atopic dermatitis and allergic urticaria are common conditions of the skin that can also be the presenting symptoms of uncommon diseases. Defects leading to immunodeficiency may be associated with atopic dermatitis or allergic urticaria. Unusually severe or otherwise atypical presentations of atopic dermatitis or allergic urticaria may lead to clinical suspicion of an underlying immunodeficiency. Published by Elsevier Inc.

Entities: Chemical Disease Gene Species

Keywords: Atopic dermatitis; Immunodeficiency; Urticaria

Mesh：

Year: 2016 PMID： 27886899 PMCID： PMC5199140 DOI： 10.1016/j.iac.2016.08.016

Source DB: PubMed Journal: Immunol Allergy Clin North Am ISSN： 0889-8561 Impact factor: 3.479

39 in total

Review 1. DOCK8 deficiency.

Authors: Helen C Su; Huie Jing; Qian Zhang
Journal: Ann N Y Acad Sci Date: 2011-12 Impact factor: 5.691

2. Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.

Authors: Lauren Staple; Timothy Andrews; Donna McDonald-McGinn; Elaine Zackai; Kathleen E Sullivan
Journal: Pediatr Allergy Immunol Date: 2005-05 Impact factor: 6.377

Review 3. PLAID: a Syndrome of Complex Patterns of Disease and Unique Phenotypes.

Authors: Joshua D Milner
Journal: J Clin Immunol Date: 2015-07-25 Impact factor: 8.317

4. Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment.

Authors: Yu Zhang; Xiaomin Yu; Mie Ichikawa; Jonathan J Lyons; Shrimati Datta; Ian T Lamborn; Huie Jing; Emily S Kim; Matthew Biancalana; Lynne A Wolfe; Thomas DiMaggio; Helen F Matthews; Sarah M Kranick; Kelly D Stone; Steven M Holland; Daniel S Reich; Jason D Hughes; Huseyin Mehmet; Joshua McElwee; Alexandra F Freeman; Hudson H Freeze; Helen C Su; Joshua D Milner
Journal: J Allergy Clin Immunol Date: 2014-02-28 Impact factor: 10.793

5. Skin infiltration of CD56(bright) CD16(-) natural killer cells in a case of X-SCID with Omenn syndrome-like manifestations.

Authors: Fumie Shibata; Tomoko Toma; Taizo Wada; Masayuki Inoue; Yumi Tone; Kazuhide Ohta; Yoshihito Kasahara; Fumie Sano; Mitsuaki Kimura; Mitsuru Ikeno; Shoichi Koizumi; Akihiro Yachie
Journal: Eur J Haematol Date: 2007-07 Impact factor: 2.997

6. Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome.

Authors: A R Gennery; M A Slatter; J Rice; L H Hoefsloot; D Barge; A McLean-Tooke; T Montgomery; J A Goodship; A D Burt; T J Flood; M Abinun; A J Cant; D Johnson
Journal: Clin Exp Immunol Date: 2008-05-26 Impact factor: 4.330

7. Comèl-Netherton syndrome defined as primary immunodeficiency.

Authors: Ellen D Renner; Dominik Hartl; Stacey Rylaarsdam; Marguerite L Young; Linda Monaco-Shawver; Gary Kleiner; M Louise Markert; E Richard Stiehm; Bernd H Belohradsky; Melissa P Upton; Troy R Torgerson; Jordan S Orange; Hans D Ochs
Journal: J Allergy Clin Immunol Date: 2009-08-14 Impact factor: 10.793

Atopic Dermatitis and Allergic Urticaria: Cutaneous Manifestations of Immunodeficiency.

Review 1. DOCK8 deficiency.

2. Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.

Review 3. PLAID: a Syndrome of Complex Patterns of Disease and Unique Phenotypes.

4. Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment.

5. Skin infiltration of CD56(bright) CD16(-) natural killer cells in a case of X-SCID with Omenn syndrome-like manifestations.

6. Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome.

7. Comèl-Netherton syndrome defined as primary immunodeficiency.

8. Familial atypical cold urticaria: description of a new hereditary disease.

Review 9. Diagnostic criteria for atopic dermatitis: a systematic review.

10. Omenn syndrome in an infant with IL7RA gene mutation.

1. Childhood atopic dermatitis: current developments, treatment approaches, and future expectations

2. The Role of Oxidative Stress in Atopic Dermatitis and Chronic Urticaria.