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TNFAIP3 mutation causing haploinsufficiency of A20 with a hemophagocytic lymphohistiocytosis phenotype: a report of two cases.
Aslani, Nahid; Asnaashari, Kosar; Parvaneh, Nima; Shahrooei, Mohammad; Sotoudeh-Anvari, Maryam; Shahram, Farhad; Ziaee, Vahid.
Affiliation
  • Aslani N; Children's Medical Center, Pediatrics Center of Excellence, Tehran, Iran.
  • Asnaashari K; Pediatric Rheumatology Society of Iran, Tehran, Iran.
  • Parvaneh N; Department of Pediatrics, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Shahrooei M; Children's Medical Center, Pediatrics Center of Excellence, Tehran, Iran.
  • Sotoudeh-Anvari M; Department of Pediatrics, Tehran University of Medical Sciences, Tehran, Iran.
  • Shahram F; Pediatric Rheumatology Research Group, Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Ziaee V; Children's Medical Center, Pediatrics Center of Excellence, Tehran, Iran.
Pediatr Rheumatol Online J ; 20(1): 78, 2022 Sep 05.
Article in En | MEDLINE | ID: mdl-36064566
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancytopenia / Cyclosporins / Lymphohistiocytosis, Hemophagocytic Type of study: Diagnostic_studies Limits: Humans / Male Language: En Journal: Pediatr Rheumatol Online J Year: 2022 Document type: Article Affiliation country: Irán Country of publication: Reino Unido
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancytopenia / Cyclosporins / Lymphohistiocytosis, Hemophagocytic Type of study: Diagnostic_studies Limits: Humans / Male Language: En Journal: Pediatr Rheumatol Online J Year: 2022 Document type: Article Affiliation country: Irán Country of publication: Reino Unido