XL-EDA-ID Presenting with Congenital Duodenal Atresia and Perforations

J Clin Immunol. 2018 Oct;38(7):733-735. doi: 10.1007/s10875-018-0544-5. Epub 2018 Aug 27.

Authors

Yusuke Mitani¹, Taizo Wada², Yusuke Matsuda¹, Seisho Sakai³, Akihiro Yachie¹

Affiliations

¹ Department of Pediatrics, School of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, 13-1 Takaramachi, Kanazawa, 920-8641, Japan.
² Department of Pediatrics, School of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, 13-1 Takaramachi, Kanazawa, 920-8641, Japan. taizo@staff.kanazawa-u.ac.jp.
³ Department of Gastroenterological Surgery, School of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan.

PMID: 30146668
DOI: 10.1007/s10875-018-0544-5

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Biomarkers
Biopsy
Duodenal Obstruction / diagnosis*
Duodenal Obstruction / genetics*
Duodenal Obstruction / surgery
Ectodermal Dysplasia / diagnosis*
Ectodermal Dysplasia / genetics*
Ectodermal Dysplasia / surgery
Genetic Diseases, X-Linked / diagnosis*
Genetic Diseases, X-Linked / genetics*
Genetic Diseases, X-Linked / surgery
Humans
Immunologic Deficiency Syndromes / diagnosis*
Immunologic Deficiency Syndromes / genetics*
Immunologic Deficiency Syndromes / surgery
Infant, Newborn
Intestinal Atresia / diagnosis*
Intestinal Atresia / genetics*
Intestinal Atresia / surgery
Intestinal Perforation / congenital*
Intestinal Perforation / diagnosis*
Intestinal Perforation / surgery
Male
Phenotype*
Primary Immunodeficiency Diseases
Radiography
Treatment Outcome

Substances

Biomarkers

Supplementary concepts

Ectodermal dysplasia, hypohidrotic, with immune deficiency
Familial duodenal atresia