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

[Familial Haemophagocytic Lymphohistiocytosis Occurs in A Fetus at His Third Trimester-A Case Report].

Zhongguo shi yan xue ye xue za zhi - 1 Dec 2017

Huang Jun-Bin, Wang Jian, Jiang Li, Wu Xiao-Jun, Chen Chun, Xu Hong-Gui, Xue Hong-Man

Abstract excerpt

OBJECTIVE: To analyze the clinical features and pathogenetic gene mutation in a fetus at his third trimester with familial haemophagocytic lymphohistiocytosis (FHL). METHODS: Target region sequencing and high-throughput sequencing were used to detect pathogenetic gene mutations for familial haemophagocytic lymphohistiocytosis in a late onset HLH fetus. Pathogenetic gene mutations of the patient and his parents...

Read the complete abstract on PubMed

Topics

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

Share to Fetus
Share to Infant, Newborn
Share to Lymphohistiocytosis, Hemophagocytic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Membrane Proteins

Share to Mutation

Share to Pregnancy

Share to Pregnancy Trimester, Third

Source

Identifiers

PMID: 29262924
DOI: 10.7534/j.issn.1009-2137.2017.06.045

Genes

FHL3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

[Familial Haemophagocytic Lymphohistiocytosis Occurs in A Fetus at His Third Trimester-A Case Report].PMID 29262924Read ↗

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

[Analysis of clinical phenotype and genetic variant in a case of familial hemophagocytic lymphohistiocytosis type Ⅲ].Semantic proximity Read ↗

Novel mutations in the UNC13D gene carried by a Chinese neonate with hemophagocytic lymphohistiocytosis.Semantic proximity Read ↗

Hemophagocytic lymphohistiocytosis with Munc13-4 mutation: a cause of recurrent fatal hydrops fetalis.Semantic proximity Read ↗

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

Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases.Semantic proximity Read ↗

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

Neonatal Primary Hemophagocytic Lymphohistiocytosis in Turkish ChildrenSemantic proximity Read ↗

A case of fetal-onset type 3 familial hemophagocytic lymphohistiocytosis surviving without severe complications after early diagnosis and treatment.Semantic proximity Read ↗

Exome sequencing detected an extremely rare case of foetal onset familial haemophagocytic lymphohistiocytosis type 5 presenting with hydrops foetalis.Semantic proximity Read ↗

Hemophagocytosis in children: when genetics gets involved…Semantic proximity Read ↗

Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHL) patients in India.Semantic proximity Read ↗

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