Nager syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
An SF3B4 mutation was found in our patient, prompting a review of the previous known cases of Rodriguez syndrome, which revealed no clustering of SF3B4 mutations, and four cases of Rodriguez syndrome with mutations identical to those in cases of Nager syndrome.
|
30924273 |
2019 |
Nager syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
A significant association with 1st-year height SD score increase during GH treatment was observed with rs11205277, located near 4 known genes: MTMR11, SV2A, HIST2H2AA3, and SF3B4; the latter, in which heterozygous mutations occur in Nager acrofacial dysostosis, appears the most relevant gene.
|
30970347 |
2019 |
Nager syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
In this work, we report a novel synonymous variant within exon 3 of the SF3B4 gene in a family with three members affected by Nager syndrome.
|
27966544 |
2017 |
Nager syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
Whole gene deletions of SF3B4 have also been suggested to be the cause of Nager syndrome in SF3B4 point mutation negative patients.
|
26679067 |
2016 |
Nager syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
This phenotype can be rescued by injection of wild-type human SF3B4 mRNA but not by mRNAs carrying mutations that cause Nager syndrome.
|
26874011 |
2016 |
Nager syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
We identified heterozygosity for SF3B4 mutations in Rodriguez syndrome, confirming that the phenotype is a dominant disorder that is allelic with Nager syndrome.
|
27622494 |
2016 |
Nager syndrome
|
0.800 |
Biomarker
|
disease |
BEFREE |
Mutations in several other genes involved in spliceosomal function or linked aspects of mRNA processing have also recently been identified in human disorders with specific craniofacial malformations: SF3B4 in Nager syndrome, an acrofacial dysostosis (AFD); SNRPB in cerebrocostomandibular syndrome, characterized by Robin sequence and rib defects; EIF4A3 in the AFD Richieri-Costa-Pereira syndrome, characterized by Robin sequence, median mandibular cleft and limb defects; and TXNL4A in Burn-McKeown syndrome, involving specific craniofacial dysmorphisms.
|
25865758 |
2015 |
Nager syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
SF3B4 is the major gene responsible for autosomal dominant Nager syndrome.
|
24003905 |
2014 |
Nager syndrome
|
0.800 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
SF3B4 is the major gene responsible for autosomal dominant Nager syndrome.
|
24003905 |
2014 |
Nager syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
Since SF3B4 mutations have been recently associated with Nager syndrome, this suggests that at least some cases of Rodriguez syndrome are either allelic to or represent unusually severe manifestations of Nager syndrome.
|
24715698 |
2014 |
Nager syndrome
|
0.800 |
Biomarker
|
disease |
BEFREE |
In our study, we performed exome sequencing in two and Sanger sequencing of SF3B4 in further ten previously unreported patients with the clinical diagnosis of Nager syndrome, including one familial case.
|
23568615 |
2013 |
Nager syndrome
|
0.800 |
GeneticVariation
|
disease |
BEFREE |
We conclude that, the presence of consanguinity and absence of mutation in SF3B4, provides evidence in support of a recessive form of Nager syndrome.
|
23913624 |
2013 |
Nager syndrome
|
0.800 |
GermlineCausalMutation
|
disease |
ORPHANET |
These results suggest that most cases of Nager syndrome are caused by haploinsufficiency of SF3B4.
|
22541558 |
2012 |
Nager syndrome
|
0.800 |
Biomarker
|
disease |
BEFREE |
These results suggest that most cases of Nager syndrome are caused by haploinsufficiency of SF3B4.
|
22541558 |
2012 |
Nager syndrome
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
These results suggest that most cases of Nager syndrome are caused by haploinsufficiency of SF3B4.
|
22541558 |
2012 |
Nager syndrome
|
0.800 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
These results suggest that most cases of Nager syndrome are caused by haploinsufficiency of SF3B4.
|
22541558 |
2012 |
Nager syndrome
|
0.800 |
Biomarker
|
disease |
CTD_human |
|
|
|
Congenital small ears
|
0.400 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major cause.
|
24003905 |
2014 |
Congenital small ears
|
0.400 |
Biomarker
|
disease |
HPO |
|
|
|
Acrofacial dysostosis Rodriguez type
|
0.300 |
GermlineCausalMutation
|
disease |
ORPHANET |
Rodriguez acrofacial dysostosis is caused by apparently de novo heterozygous mutations in the SF3B4 gene.
|
27642715 |
2016 |
Multiple congenital anomalies
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Rodriguez acrofacial dysostosis is caused by apparently de novo heterozygous mutations in the SF3B4 gene.
|
27642715 |
2016 |
Dysmorphic features
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Rodriguez acrofacial dysostosis is caused by apparently de novo heterozygous mutations in the SF3B4 gene.
|
27642715 |
2016 |
Multiple congenital anomalies
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Rodriguez syndrome with SF3B4 mutation: a severe form of Nager syndrome?
|
24715698 |
2014 |
Multiple congenital anomalies
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major cause.
|
24003905 |
2014 |
Dysmorphic features
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Rodriguez syndrome with SF3B4 mutation: a severe form of Nager syndrome?
|
24715698 |
2014 |