Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Diagnostic challenges in a child with familial hemophagocytic lymphohistiocytosis type 3 (FHLH3) presenting with fulminant neurological disease.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery - 1 Feb 2009

Weisfeld-Adams James D, Frank Yitzchak, Havalad Vinod, Hojsak Joanne M, Posada Roberto, Kaicker Shipra M, Wistinghausen Birte

Abstract excerpt

BACKGROUND: Familial hemophagocytic lymphohistiocytosis (FHLH) is an autosomal recessively inherited multisystem disease characterized by fever, rash, splenomegaly, cytopenias, and variable central nervous system (CNS) manifestations. CASE HISTORY: We report the case of a 3-year-old boy who presented with splenomegaly and normocytic anemia 4 months after returning to the US from a region endemic for Leishmania...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anemia
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Demyelinating Diseases

Share to Diagnosis, Differential

Share to Lymphohistiocytosis, Hemophagocytic

Share to Membrane Proteins

Share to Mutation

Share to Splenomegaly

Source

Identifiers

PMID: 19023578
DOI: 10.1007/s00381-008-0744-z

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Diagnostic challenges in a child with familial hemophagocytic lymphohistiocytosis type 3 (FHLH3) presenting with fulminant neurological disease.PMID 19023578Read ↗

Clinical and neuroimaging features of familial hemophagocytic lymphohistiocytosis.Semantic proximity Read ↗

Atypical familial hemophagocytic lymphohistiocytosis type 3 in children: A report of cases and literature review.Semantic proximity Read ↗

Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic review.Semantic proximity Read ↗

Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic Lymphohistiocytosis.Semantic proximity Read ↗

Familial hemophagocytic lymphohistiocytosis in a neonate: Case report and literature review.Semantic proximity Read ↗

Familial hemophagocytic lymphohistiocytosis in a pediatric patient diagnosed by brain magnetic resonance imaging.Semantic proximity Read ↗

Familial haemophagocytosis lymphohisticytosis type 3: A case report.Semantic proximity Read ↗

Pediatric Hemophagocytic Lymphohistiocytosis Presenting as a Refractory Febrile Illness: A CASE REPORTSemantic proximity Read ↗

Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3.Semantic proximity Read ↗

Neurological symptoms of familial hemophagocytic lymphohistiocytosis type 2.Semantic proximity Read ↗

Allogeneic hematopoietic stem cell transplant for familial hemophagocytic lymphohistiocytosis: a case report and literature review.Semantic proximity Read ↗

Detection of a novel gross deletion in the UNC13D gene ends the diagnostic odyssey for a family with familial hemophagocytic lymphohistiocytosis 3Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.