A case of anhidrotic ectodermal dysplasia presenting with pyrexia, atopic eczema, and food allergy.

Anhidrotic ectodermal dysplasia Chronic eczema Food allergy Pyrexia

Journal

Asia Pacific allergy
ISSN: 2233-8276
Titre abrégé: Asia Pac Allergy
Pays: Netherlands
ID NLM: 101561954

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 10 12 2018
accepted: 10 01 2019
entrez: 12 2 2019
pubmed: 12 2 2019
medline: 12 2 2019
Statut: epublish

Résumé

Anhidrotic ectodermal dysplasia (AED) is a rare hereditary disorder with a triad of sparse hair, dental hypoplasia, and anhidrosis. Here we report a case of AED with food allergy and atopic eczema. The patient was a 11-month-old boy admitted to our hospital with pyrexia for 2 weeks. He presented with a history of dry skin, eczema, and food allergy to egg. On clinical examination, his body temperature was 38.8°C, with dry skin and eczema almost all over the body, sparse eyebrows, and scalp hair. Laboratory investigations and physical examination did not show any evidence of infection. Radioallergosorbent test was positive to egg yolk, egg white, ovomucoid, milk, house dust, and house dust mite. As the child did not sweat despite the high fever, we performed the sweat test which revealed a total lack of sweat glands. Genetic examination revealed a mutation of the

Identifiants

pubmed: 30740351
doi: 10.5415/apallergy.2019.9.e3
pii: 2019090109
pmc: PMC6365661
doi:

Types de publication

Case Reports

Langues

eng

Pagination

e3

Déclaration de conflit d'intérêts

Conflict of Interest: The authors have no financial conflicts of interest.

Références

Acta Derm Venereol. 2015 Apr;95(4):476-9
pubmed: 25270765
J Hum Genet. 2016 Oct;61(10):891-897
pubmed: 27305980
Ann Allergy Asthma Immunol. 2012 Jun;108(6):435-8
pubmed: 22626597
Eur J Med Genet. 2011 Jul-Aug;54(4):e377-82
pubmed: 21457804
Cytokine Growth Factor Rev. 2014 Apr;25(2):195-203
pubmed: 24508088
Arch Dis Child. 1987 Oct;62(10):989-96
pubmed: 2445301
J Appl Genet. 2016 Feb;57(1):51-61
pubmed: 26294279
Arch Dis Child. 1929 Aug;4(22):215-26
pubmed: 21031766

Auteurs

Tamaho Suzuki (T)

Department of Pediatrics, Nippon Medical School Musashi Kosugi Hospital, Kanagawa, Japan.

Hanako Tajima (H)

Department of Pediatrics, Nippon Medical School Musashi Kosugi Hospital, Kanagawa, Japan.

Makoto Migita (M)

Department of Pediatrics, Nippon Medical School Hospital, Tokyo, Japan.

Ruby Pawankar (R)

Department of Pediatrics, Nippon Medical School Hospital, Tokyo, Japan.

Takeshi Yanagihara (T)

Department of Pediatrics, Nippon Medical School Musashi Kosugi Hospital, Kanagawa, Japan.

Atsushi Fujita (A)

Department of Pediatrics, Nippon Medical School Musashi Kosugi Hospital, Kanagawa, Japan.

Yoshio Shima (Y)

Department of Pediatrics, Nippon Medical School Musashi Kosugi Hospital, Kanagawa, Japan.

Emi Yanai (E)

Department of Pediatrics, Nippon Medical School Musashi Kosugi Hospital, Kanagawa, Japan.

Yasuhiko Katsube (Y)

Department of Pediatrics, Nippon Medical School Musashi Kosugi Hospital, Kanagawa, Japan.

Classifications MeSH