Evidence map›Paper›PMID 27033759›Full record

ArticleZhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi2016

[Clinical and genetic features of dyskeratosis congenital with bone marrow failure in eight patients].

Y Wan, W B An, J Y Zhang, J L Zhang, R R Zhang, S Zhu, L X Chang, Y C Zhang, F Liu, W Y Yang and 4 more

Open access · greenAbstract read
In one paragraph

Article in Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 98% of its field
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

14 authors at 1 institution in 1 country.

Y WanCenter of Pediatric Blood Diseases, Institute of Hematology and Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
W B An
J Y Zhang
J L Zhang
R R Zhang
S Zhu
L X Chang
Y C Zhang
F Liu
W Y Yang
X J Chen
Y Zou
Y M Chen
X F Zhu
Institute of Hematology & Blood Diseases Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo summary clinical and genetic features of childhood dyskeratosis congenital (DC) patients with bone marrow failure.

methodsThe clinical data of 8 DC patients with bone marrow failure diagnosed between September 2010 and September 2015 were collected. Whole exons with flanking regions of the 16 telomere-related genes, including DKC1, TERC, TERT, NOP10, NHP2, TINF2 and so on, were analyzed by next generation sequence.

resultsSix males and two females were included, with a median age of 42(15-60) months. The median blood cell count at onset were as follow: WBC 3.99 (1.26-5.44) × 10(9)/L, ANC 1.11 (0.38-2.15) × 10(9)/L, RBC 2.45 (0.37-3.56) × 10(12)/L, HGB 82.5(15-127) g/L, PLT 27 (2-112) ×10(9)/L. Hypoplastic or marked hypoplastic bone marrow were seen in 6 patients. DKC1 mutiaton were indentified in 3 patients: one c.961C>A mutation, and two c.1058C>T mutation. TINF2 mutations were identified in 4 patients: c.849delC, c.844C>T, c.811C>T, c.862T>A combined c.871delA. One patient had TINF2 mutation c.848C>A combined TERT mutation c.1138C>T. DKC1 c.961C>A mutation, TINF2 c.849delC mutation and TINF2 c.871delA mutaion were not reported so far. 5 of 7 patients got better after androgen administration. During follow-up, one patient died of serious infection, the other seven patients continued the treatment.

conclusionsTINF2 and DKC1 mutations were the main genetic phenotypes in childhood DC with marrow failure patients. Androgen is effetive in some cases.

Indexed as

Bone MarrowCell Cycle ProteinsChild, PreschoolDNA Mutational AnalysisDyskeratosis CongenitaExonsFemaleHumansInfantMaleMutationNuclear ProteinsPancytopeniaTelomeraseTelomere-Binding ProteinsCell Cycle ProteinsDKC1 protein, humanNuclear ProteinsTelomeraseTelomere-Binding ProteinsTERT protein, humanTINF2 protein, human

Identifiers

PMID27033759
PMCPMC7342957
OpenAlexW2316824316

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LicenceCC BY-NC-SA
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.