المؤلفون: Valeri L; Department of Medical and Surgical Sciences of the Mothers, Children and Adults, Post Graduate School of Paediatrics, University of Modena and Reggio Emilia, Modena, Italy., Lugli L; Neonatology Unit, Mother-Child Department, University Hospital of Modena, Modena, Italy., Iughetti L; Department of Medical and Surgical Sciences of the Mothers, Children and Adults, Post Graduate School of Paediatrics, University of Modena and Reggio Emilia, Modena, Italy., Soresina A; Unit of Pediatric Immunology, Pediatrics Clinic, ASST-Spedali Civili of Brescia, Brescia, Italy., Giliani S; Cytogenetic and Medical Genetics Unit, 'A. Nocivelli' Institute for Molecular Medicine, Spedali Civili Hospital, Brescia, Italy., Porta F; Pediatric Oncohematology and Bone Marrow Transplant Unit, Children's Hospital, Spedali Civili, Brescia, Italy., Berardi A; Neonatology Unit, Mother-Child Department, University Hospital of Modena, Modena, Italy.

المصدر: Pediatrics [Pediatrics] 2022 Jan 01; Vol. 149 (1).

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: American Academy of Pediatrics Country of Publication: United States NLM ID: 0376422 Publication Model: Print Cited Medium: Internet ISSN: 1098-4275 (Electronic) Linking ISSN: 00314005 NLM ISO Abbreviation: Pediatrics Subsets: MEDLINE

مواضيع طبية MeSH: Frameshift Mutation* , Siblings*, Homeodomain Proteins/*genetics , Hydrops Fetalis/*etiology , Severe Combined Immunodeficiency/*diagnosis , Severe Combined Immunodeficiency/*genetics, Alopecia/complications ; Dermatitis, Exfoliative/complications ; Homozygote ; Humans ; Infant, Newborn ; Male ; Morocco ; Pedigree ; Severe Combined Immunodeficiency/complications