Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases.

Sadeghi, Payman; Esslami, Golnaz Ghazizadeh; Rokni-Zadeh, Hassan; Changi-Ashtiani, Majid; Mohsenipour, Reihaneh

Sadeghi, Payman; Esslami, Golnaz Ghazizadeh; Rokni-Zadeh, Hassan; Changi-Ashtiani, Majid; Mohsenipour, Reihaneh.

Afiliación

Sadeghi P; Children's Medical Center, Pediatrics Center of Excellence, Tehran, Iran.
Esslami GG; Department of Pediatrics, Tehran University of Medical Sciences, Tehran, Iran.
Rokni-Zadeh H; Pediatric Rheumatology Society of Iran, Tehran, Iran.
Changi-Ashtiani M; Department of Emergency, Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
Mohsenipour R; Departments of Newborn Nursery, Neonates and Pediatrics, Ziaeian Hospital, Tehran University of Medical Sciences, Tehran, Iran.

BMC Pediatr ; 22(1): 667, 2022 11 19.

Article en En | MEDLINE | ID: mdl-36401200

Asunto(s)

Linfohistiocitosis Hemofagocítica; Masculino; Humanos; Femenino; Recién Nacido; Lactante; Linfohistiocitosis Hemofagocítica/diagnóstico; Linfohistiocitosis Hemofagocítica/genética; Mutación; Homocigoto; Triglicéridos; Ferritinas; Proteínas de la Membrana/genética

Palabras clave

Case report; FHL (familial Hemophagocytic lymphohistiocytosis); HLH (Hemophagocytic lymphohistiocytosis); UNC13D

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Linfohistiocitosis Hemofagocítica Tipo de estudio: Diagnostic_studies / Guideline Límite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: BMC Pediatr Asunto de la revista: PEDIATRIA Año: 2022 Tipo del documento: Article País de afiliación: Irán

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