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Recurrent Infections and Immunodeficiency Caused by Severe Pancytopenia Associated with a Novel Life-Threatening Mutation in Hypoxia-Upregulated Protein 1.
Jafari Khamirani, Hossein; Dianatpour, Mehdi; Zoghi, Sina; Mohammadi, Sanaz; Habib, Ashkan; Dastgheib, Seyed Alireza; Tabei, Seyed Mohammad Bagher; Molayemat, Mohadeseh; Shirazi Yeganeh, Babak.
Afiliación
  • Jafari Khamirani H; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Dianatpour M; Comprehensive Medical Genetic Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Zoghi S; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Mohammadi S; Stem Cells Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Habib A; Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Dastgheib SA; Comprehensive Medical Genetic Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Tabei SMB; Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Molayemat M; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Shirazi Yeganeh B; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.
Immunol Invest ; 51(6): 1883-1894, 2022 Aug.
Article en En | MEDLINE | ID: mdl-35549617
ABSTRACT
HYOU1 encodes a protein from the endoplasmic reticulum chaperone proteins, expressed to protect cellular mechanisms from stress such as hypoxia, insufficient energy and excessive or insufficient substances, and to restore cell homeostasis. In this study, we report a novel pathogenic variant in HYOU1. The proband, the second patient with pathogenic variant in HYOU1, was a female born to consanguineous parents. A novel homozygous pathogenic variant in HYOU1 (NM_001130991.3 c.1456C>T; p.Arg486Cys) was identified, causing anemia, thrombocytopenia and severe panleukopenia and immunodeficiency in the second month of age, leading to consistent high-grade fever, regression of brain functions and recurrent infections; ultimately resulting in the patient expiring at three and half months of age. Both parents are heterozygous for this variant and have no issues related to this study.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pancitopenia / Proteínas HSP70 de Choque Térmico / Síndromes de Inmunodeficiencia Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Infant Idioma: En Revista: Immunol Invest Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Irán

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pancitopenia / Proteínas HSP70 de Choque Térmico / Síndromes de Inmunodeficiencia Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Infant Idioma: En Revista: Immunol Invest Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Irán