First reported case of Omenn syndrome in a patient with reticular dysgenesis

Henderson, Lauren A.; Frugoni, Francesco; Hopkins, Gregory; Al-Herz, Waleed; Weinacht, Katja; Comeau, Anne Marie; Bonilla, Francisco A.; Notarangelo, Luigi D.; Pai, Sung-Yun

doi:10.1016/j.jaci.2012.07.045

i

First reported case of Omenn syndrome in a patient with reticular dysgenesis

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September 24 2012
By Henderson, Lauren A. ; Frugoni, Francesco ; Hopkins, Gregory ; ...

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English

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Alternative Title:

J Allergy Clin Immunol
Personal Author:

Henderson, Lauren A. ; Frugoni, Francesco ; Hopkins, Gregory ; Al-Herz, Waleed ; Weinacht, Katja ; Comeau, Anne Marie ; Bonilla, Francisco A. ; Notarangelo, Luigi D. ; Pai, Sung-Yun
Subjects:

Adenylate Kinase Article Consanguinity Humans Infant, Newborn Leukopenia Male Mutation Severe Combined Immunodeficiency T-Lymphocytes
Source:

J Allergy Clin Immunol. 131(4):1227-1230.e3
Pubmed ID:

23014587
Pubmed Central ID:

PMC3894621
Document Type:

Journal Article
Funding:

U54 AI082973/AI/NIAID NIH HHS/United States ; U54AI082973/AI/NIAID NIH HHS/United States ; 1U01EH00362/EH/NCEH CDC HHS/United States
Volume:

131
Issue:

4
Collection(s):

CDC Public Access
Main Document Checksum:

urn:sha256:a70f282b071ab7656c9e00c59a90371770af79f0776ec97fecf28c9f5cd7f792
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https://stacks.cdc.gov/view/cdc/33653/cdc_33653_DS1.pdf
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[PDF - 306.87 KB ]

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