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Article

Familial hemophagocytic lymphohistiocytosis in a 6-week-old male infant.

Collegium antropologicum - 1 Jun 2010

Jakovljević Gordana, Kardum-Skelin Ika, Rogosić Srdan, Culić Srdana, Stepan Jasminka, Gagro Alenka, Skarić Ivancica, Mikecin Lili, Bonevski Aleksandra, Barisić Ingeborg, Nakić Melita

Abstract excerpt

Familial hemophagocytic lymphohistiocytosis (FLH) is an autosomal recessively inherited multisystem disease. This defect in cellular cytotoxicity is a life threatening condition characterized by fever, rash, splenomegaly, cytopenias and neurologic manifestations. PRF1, UNC13D and STX11 gene defec...

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Source

Identifiers

PMID: 20698142

Genes

PRF1
STX11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20698142-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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