Okihiro Syndrome
|
1.000 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Okihiro Syndrome
|
1.000 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Okihiro Syndrome
|
1.000 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Acro-renal-ocular syndrome: autosomal dominant thumb hypoplasia, renal ectopia, and eye defect.
|
6426304 |
1984 |
Okihiro Syndrome
|
1.000 |
Biomarker
|
disease |
BEFREE |
Prominent expression in the developing midbrain, branchial arches and the limbs suggests an important function of SALL4 during development of these structures as expected from the observation in Okihiro syndrome patients.
|
12826753 |
2002 |
Okihiro Syndrome
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Okihiro syndrome is caused by SALL4 mutations.
|
12393809 |
2002 |
Okihiro Syndrome
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family.
|
12395297 |
2002 |
Okihiro Syndrome
|
1.000 |
GeneticVariation
|
disease |
UNIPROT |
Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family.
|
12395297 |
2002 |
Okihiro Syndrome
|
1.000 |
GeneticVariation
|
disease |
UNIPROT |
Okihiro syndrome is caused by SALL4 mutations.
|
12393809 |
2002 |
Okihiro Syndrome
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Furthermore we confirm the overlap of acro-renal-ocular syndrome with Okihiro syndrome at the molecular level and expand the phenotype of SALL4 mutations.
|
12843316 |
2003 |
Okihiro Syndrome
|
1.000 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Furthermore we confirm the overlap of acro-renal-ocular syndrome with Okihiro syndrome at the molecular level and expand the phenotype of SALL4 mutations.
|
12843316 |
2003 |
Okihiro Syndrome
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
SALL4 mutations may also cause acro-renal-ocular syndrome (AROS), which differs from DRRS by the presence of structural eye anomalies, and phenotypes similar to thalidomide embryopathy and Holt-Oram syndrome (HOS).
|
16086360 |
2005 |
Okihiro Syndrome
|
1.000 |
GermlineCausalMutation
|
disease |
ORPHANET |
SALL4 mutations may also cause acro-renal-ocular syndrome (AROS), which differs from DRRS by the presence of structural eye anomalies, and phenotypes similar to thalidomide embryopathy and Holt-Oram syndrome (HOS).
|
16086360 |
2005 |
Okihiro Syndrome
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
This finding illustrates that the phenotypic and functional effects of SALL4 missense mutations are difficult to predict, and that other SALL4 missense mutations might lead to phenotypes not overlapping with Okihiro syndrome.
|
16402211 |
2006 |
Okihiro Syndrome
|
1.000 |
GeneticVariation
|
disease |
UNIPROT |
This finding illustrates that the phenotypic and functional effects of SALL4 missense mutations are difficult to predict, and that other SALL4 missense mutations might lead to phenotypes not overlapping with Okihiro syndrome.
|
16402211 |
2006 |
Okihiro Syndrome
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Mutations in SALL4 have been identified in patients with Okihiro syndrome, which is characterized by radial ray anomalies associated with a Duane anomaly.
|
16411190 |
2006 |
Okihiro Syndrome
|
1.000 |
Biomarker
|
disease |
MGD |
Furthermore, we demonstrated that anorectal and heart anomalies in Okihiro syndrome are caused by Sall4 haploinsufficiency and that Sall4/Sall1 heterozygotes exhibited an increased incidence of anorectal and heart anomalies, exencephaly and kidney agenesis.
|
16790473 |
2006 |
Okihiro Syndrome
|
1.000 |
Biomarker
|
disease |
CTD_human |
This finding illustrates that the phenotypic and functional effects of SALL4 missense mutations are difficult to predict, and that other SALL4 missense mutations might lead to phenotypes not overlapping with Okihiro syndrome.
|
16402211 |
2006 |
Okihiro Syndrome
|
1.000 |
Biomarker
|
disease |
MGD |
Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart.
|
16380715 |
2006 |
Okihiro Syndrome
|
1.000 |
Biomarker
|
disease |
BEFREE |
Here we report the detection and molecular characterization of four novel, overlapping microdeletions, all spanning SALL4 and flanking genes, in four unrelated cases with features of Okihiro syndrome and variable degrees of psychomotor delay.
|
17623483 |
2007 |
Okihiro Syndrome
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
The authors examined four male and two female affected members of a pedigree previously reported to cosegregate DRRS and a heterozygous SALL4 mutation.
|
18055799 |
2007 |
Okihiro Syndrome
|
1.000 |
Biomarker
|
disease |
MGD |
Truncating mutations in SALL4 cause Okihiro syndrome, manifest as Duane anomaly, radial ray defects and sensorineural and conductive deafness.
|
17216607 |
2007 |
Okihiro Syndrome
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
SAL-Like 4 (SALL4) gene mutations have been identified to be the cause of Okihiro syndrome which is characterized by association limb and multiple other organ developmental defects including heart defect.
|
19619907 |
2010 |
Okihiro Syndrome
|
1.000 |
GeneticVariation
|
disease |
BEFREE |
Recently mutations of the SALL4 gene on chromosome 20 have been linked to DRS associated with radial forearm malformations (Okihiro syndrome).
|
21405998 |
2011 |
Okihiro Syndrome
|
1.000 |
Biomarker
|
disease |
BEFREE |
Typically, SALL4-related Duane-radial ray syndrome is caused by deletions or nonsense mutations; the only missense SALL4 mutation described prior was thought to result in gain of function and produced cranial midline defects.
|
25823593 |
2015 |
Okihiro Syndrome
|
1.000 |
CausalMutation
|
disease |
CLINVAR |
Novel frameshift variant in gene SALL4 causing Okihiro syndrome.
|
26791099 |
2016 |