17q12 Kennisbankdeletion syndrome · static snapshot
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Nieuwe bevindingen

Alles wat de analyse-engine uit het corpus afleidde: nieuwe publicaties, gewijzigde bronnen, gen–kenmerk-koppelingen, gerapporteerde cijfers, zorgaanbevelingen en tegenstrijdig bewijs. Elke kaart toont hoeveel onafhankelijke bronnen het ondersteunen en linkt naar de exacte zin.

Fenotype-uitbreiding nieren en urineleider conf 97%

Nieuwe waarneming gerapporteerd: The discovery of novel GCK mutations represents a major strength of this study, as this gene exhibits one of t…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “The discovery of novel GCK mutations represents a major strength of this study, as this gene exhibits one of the most heterogeneous mutational spectra among all MODY-related genes, with more than 600 distinct variants described worldwide [ 32 , 38 ].”

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Fenotype-uitbreiding nieren en urineleider conf 97%

Nieuwe waarneming gerapporteerd: 12 In this study, we reported an extremely rare case of simultaneous presentation of MRKH syndrome, left ingui…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “12 In this study, we reported an extremely rare case of simultaneous presentation of MRKH syndrome, left inguinal hernia, and left renal fusion with malrotation, and reported our experience in the diagnosis and treatment of such conditions.”

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Fenotype-uitbreiding nieren en urineleider conf 97%

Nieuwe waarneming gerapporteerd: Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agene…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.”

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Fenotype-uitbreiding nieren en urineleider conf 97%

Nieuwe waarneming gerapporteerd: This study aimed to evaluate the genetic and clinical features of pediatric patients with MODY, to assess the …

Een bron beschrijft een nieuwe of uitgebreide waarneming: “This study aimed to evaluate the genetic and clinical features of pediatric patients with MODY, to assess the prevalence of common and rare subtypes, and to report novel pathogenic variants identified in a Turkish cohort.”

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Fenotype-uitbreiding nieren en urineleider conf 97%

Nieuwe waarneming gerapporteerd: The objectives were to define the clinical and phenotypic variability within this cohort, identify previously …

Een bron beschrijft een nieuwe of uitgebreide waarneming: “The objectives were to define the clinical and phenotypic variability within this cohort, identify previously unreported (novel) mutations, and determine the prevalence of rare MODY subtypes.”

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Fenotype-uitbreiding Klachten & kenmerken conf 97%

Nieuwe waarneming gerapporteerd: We report five patients with Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS), four of whom presented with prec…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “We report five patients with Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS), four of whom presented with precocious puberty and one with growth hormone deficiency (GHD.”

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Fenotype-uitbreiding Onderzoeksgrens conf 97%

Nieuwe waarneming gerapporteerd: CONCLUSIONS Existing disease candidate gene prioritization methodologies mine biological and functional inform…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “CONCLUSIONS Existing disease candidate gene prioritization methodologies mine biological and functional information about candidate genes, and we believe that our ToppGene Suite can complement these existing approaches by applying novel methods that mine...

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Fenotype-uitbreiding nieren en urineleider conf 97%

Nieuwe waarneming gerapporteerd: The most intriguing and novel finding in our study is the unexpected postnatal complete sonographic resolution…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “The most intriguing and novel finding in our study is the unexpected postnatal complete sonographic resolution of renal parenchymal hyperechogenicity, without evolution to cystic changes among unsuspected prenatal cases.”

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Fenotype-uitbreiding nieren en urineleider conf 97%

Nieuwe waarneming gerapporteerd: Another novel finding among our patients is the coexistence of both types of HNF1B- associated kidney abnormal…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “Another novel finding among our patients is the coexistence of both types of HNF1B- associated kidney abnormalities, i.e., cystic kidneys and CAKUT, which presented sequentially in Patient 3.”

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Fenotype-uitbreiding Klachten & kenmerken conf 97%

Nieuwe waarneming gerapporteerd: Although MIEN1 is regarded as a novel gene involved in prostate cancer progression by enhancing cell migration…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “Although MIEN1 is regarded as a novel gene involved in prostate cancer progression by enhancing cell migration and invasion, the relative functional significance and regulatory mechanisms of MIEN1 remain largely unknown.”

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Fenotype-uitbreiding leren, taal en gedrag conf 97%

Nieuwe waarneming gerapporteerd: Discussion and conclusions Here we reported a 17-year-old Chinese juvenile who was suffering from ACC with com…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “Discussion and conclusions Here we reported a 17-year-old Chinese juvenile who was suffering from ACC with comorbid social anxiety disorder, and accompanied by behavior problems, psychiatric symptoms.”

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Fenotype-uitbreiding leren, taal en gedrag conf 97%

Nieuwe waarneming gerapporteerd: That is, children with high behavioral inhibition (BI), which refers to caution, fear, low rate of approach, a…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “That is, children with high behavioral inhibition (BI), which refers to caution, fear, low rate of approach, and passive withdrawal in novel situations [ 39 ], may evolve to social phobia in their growth.”

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Fenotype-uitbreiding leren, taal en gedrag conf 97%

Nieuwe waarneming gerapporteerd: Prenatal identification of a novel mutation in the MCPH1 gene associated with autosomal recessive primary micr…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “Prenatal identification of a novel mutation in the MCPH1 gene associated with autosomal recessive primary microcephaly (MCPH) using next generation sequencing (NGS): a case report and review of the literature.”

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Fenotype-uitbreiding leren, taal en gedrag conf 97%

Nieuwe waarneming gerapporteerd: 36 Importantly, NGS performed on CVS samples has enabled the identification of rare monogenic disorders, inclu…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “36 Importantly, NGS performed on CVS samples has enabled the identification of rare monogenic disorders, including a novel MCPH1 mutation associated with autosomal recessive primary microcephaly, highlighting the value of early sampling combined with...

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Fenotype-uitbreiding nieren en urineleider conf 97%

Nieuwe waarneming gerapporteerd: We report the case of a 60-year-old Japanese woman with genetically confirmed maturity-onset diabetes of the y…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “We report the case of a 60-year-old Japanese woman with genetically confirmed maturity-onset diabetes of the young type 5 [MODY5; HNF1B (hepatocyte nuclear factor 1B)-MODY] who developed amyotrophic lateral sclerosis (ALS), a progressive neurodegenerative disorder.”

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Fenotype-uitbreiding Klachten & kenmerken conf 97%

Nieuwe waarneming gerapporteerd: This disorder has an incidence of approximately 1 in 4500 newborn girls and the aetiology is poorly understood…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “This disorder has an incidence of approximately 1 in 4500 newborn girls and the aetiology is poorly understood. we report on two patients affected by MRKH syndrome in which array-CGH analysis disclosed an identical deletion spanning 1.5 Mb of genomic DNA at...

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Fenotype-uitbreiding nieren en urineleider conf 97%

Nieuwe waarneming gerapporteerd: Emerging evidence describes a "paradoxical" phenomenon where specific LoF mutations, initially causing hyperin…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “Emerging evidence describes a "paradoxical" phenomenon where specific LoF mutations, initially causing hyperinsulinemic hypoglycemia in infancy, predispose individuals to glucose intolerance or frank diabetes in later life, often classified as...

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Fenotype-uitbreiding nieren en urineleider conf 97%

Nieuwe waarneming gerapporteerd: Emerging evidence suggests that GLP-1 receptor agonists can mitigate ER stress and preserve remaining β-cell f…

Een bron beschrijft een nieuwe of uitgebreide waarneming: “Emerging evidence suggests that GLP-1 receptor agonists can mitigate ER stress and preserve remaining β-cell function, shifting the management paradigm from pure insulin replacement to disease-modifying therapy [ 43 ].”

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Frequentie / cijfer leren, taal en gedrag conf 97%

Exome-wide burden analysis To evaluate the excess of rare, deleterious protein-coding variants in individuals with epile

Een bron meldt “0.005%” in de context van leren, taal en gedrag: “Exome-wide burden analysis To evaluate the excess of rare, deleterious protein-coding variants in individuals with epilepsy, we performed burden analysis across the entire exome, at both an individual-gene and a gene-set level. "Ultra-rare" variants...

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Frequentie / cijfer leren, taal en gedrag conf 97%

This resulted in 48,767 samples (~90% of initial) for the downstream burden analysis, which comprises 18,963 epilepsy ca

Een bron meldt “90%” in de context van leren, taal en gedrag: “This resulted in 48,767 samples (~90% of initial) for the downstream burden analysis, which comprises 18,963 epilepsy cases (including 1,743 DEEs, 4,980 GGE, and 8,425 NAFE) and 29,804 controls.”

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Frequentie / cijfer leren, taal en gedrag conf 97%

After stringent quality control (QC; Methods ), we included a total of 20,979 individuals with epilepsy and 33,444 contr

Een bron meldt “979 individuals” in de context van leren, taal en gedrag: “After stringent quality control (QC; Methods ), we included a total of 20,979 individuals with epilepsy and 33,444 controls without known neurological or neuropsychiatric conditions in our URV association analysis, roughly doubling the...

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Frequentie / cijfer leren, taal en gedrag conf 97%

We performed the association analyses separately for each epilepsy subtype - including 1,938 individuals with a diagnosi

Een bron meldt “938 individuals” in de context van leren, taal en gedrag: “We performed the association analyses separately for each epilepsy subtype - including 1,938 individuals with a diagnosis of a DEE, 5,499 with GGE, and 9,219 with NAFE - as well as for all epilepsy-affected individuals combined (including an...

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Frequentie / cijfer Onderzoeksgrens conf 97%

It is reported that the incidences of transient non-visualization, GB agenesis, biliary atresia, cystic fibrosis and chr

Een bron meldt “69.4%” in de context van algemeen: “It is reported that the incidences of transient non-visualization, GB agenesis, biliary atresia, cystic fibrosis and chromosomal abnormalities of isolated NVFGB in western populations were 69.4%, 24.7%, 3.5%, 2.4% and 1.4%, respectively [ 6 ].”

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Frequentie / cijfer Onderzoeksgrens conf 97%

An additional genetic analysis was reported for 15 individuals with recurrent duplications and duplications larger than

Een bron meldt “15 individuals” in de context van algemeen: “An additional genetic analysis was reported for 15 individuals with recurrent duplications and duplications larger than 1 Mb: three had single nucleotide variants of uncertain clinical significance, one had a pathogenic 15q11.2 deletion, and the remaining 11 h”

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Frequentie / cijfer nieren en urineleider conf 97%

We have therefore founded the Aetiology of renal and urinary tract anomalies defines Diagnostic Efficacy and Clinical Ou

Een bron meldt “3750 individuals” in de context van nieren en urineleider: “We have therefore founded the Aetiology of renal and urinary tract anomalies defines Diagnostic Efficacy and Clinical Outcome (ArtDECO) consortium, a large translational research framework within the Netherlands that includes a data- and...

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Frequentie / cijfer nieren en urineleider conf 97%

To visualize this complexity of assigning genetic causality in CAKUT, Martino et al. calculated incredible estimates of

Een bron meldt “384 cases” in de context van nieren en urineleider: “To visualize this complexity of assigning genetic causality in CAKUT, Martino et al. calculated incredible estimates of 93,384 cases and 9,244,968 controls needed to identify genome-wide significant associations in a theoretical but feasible...

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Frequentie / cijfer leren, taal en gedrag conf 97%

However, Ricardo et al. used SPECT to analyze rCBF in areas such as the frontal, temporal, and parietal cortex in 21 pat

Een bron meldt “21 patients” in de context van leren, taal en gedrag: “However, Ricardo et al. used SPECT to analyze rCBF in areas such as the frontal, temporal, and parietal cortex in 21 patients with POE and 23 patients with epilepsy and found no differences [ 65 ].”

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Frequentie / cijfer leren, taal en gedrag conf 97%

A meta-analysis conducted in 2023, encompassing 8256 individuals diagnosed with schizophrenia and 7532 healthy individua

Een bron meldt “8256 individuals” in de context van leren, taal en gedrag: “A meta-analysis conducted in 2023, encompassing 8256 individuals diagnosed with schizophrenia and 7532 healthy individuals, revealed significantly reduced levels of glutamate in the medial frontal cortex, elevated levels of glutamine in the...

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Frequentie / cijfer leren, taal en gedrag conf 97%

One study found that 11% of patients in two large epilepsy cohorts had antibodies against autoantigens, such as NMDA rec

Een bron meldt “11%” in de context van leren, taal en gedrag: “One study found that 11% of patients in two large epilepsy cohorts had antibodies against autoantigens, such as NMDA receptors, voltage-gated potassium channel complex protein, glycine receptors, and glutamic acid decarboxylase [ 145 ].”

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Frequentie / cijfer leren, taal en gedrag conf 97%

A systematic review of 58 valid articles showed that patients with epilepsy had a pooled odds ratio for risk of 7.8 for

Een bron meldt “5.6%” in de context van leren, taal en gedrag: “A systematic review of 58 valid articles showed that patients with epilepsy had a pooled odds ratio for risk of 7.8 for developing psychosis compared with controls, and the pooled prevalence was estimated to be 5.6% (95%CI: 4.8-6.4%).”

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Frequentie / cijfer leren, taal en gedrag conf 97%

In addition, the prevalence of psychotic disorders in temporal lobe epilepsy (TLE) is even higher, with an estimated 7%

Een bron meldt “7%” in de context van leren, taal en gedrag: “In addition, the prevalence of psychotic disorders in temporal lobe epilepsy (TLE) is even higher, with an estimated 7% (95% CI: 4.9-9.1%) [ 6 ], whereas the probability of psychotic disorders in extra-TLE is about 4.3% [ 7 ].”

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Frequentie / cijfer leren, taal en gedrag conf 97%

A 1-year follow-up of 12 patients with chronic interictal psychosis combined with intractable epilepsy showed that four

Een bron meldt “12 patients” in de context van leren, taal en gedrag: “A 1-year follow-up of 12 patients with chronic interictal psychosis combined with intractable epilepsy showed that four patients worsened at 6 months and 1 year after treatment, two patients deteriorated at 6 months and improved at 1 year, three...

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Frequentie / cijfer leren, taal en gedrag conf 97%

A large cohort of 50 patients with POE and 50 patients with epilepsy examined the volume of the total hippocampus and ea

Een bron meldt “50 patients” in de context van leren, taal en gedrag: “A large cohort of 50 patients with POE and 50 patients with epilepsy examined the volume of the total hippocampus and each subregion and found that the volumes of the posterior hippocampus were reduced bilaterally in POE patients.”

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Frequentie / cijfer nieren en urineleider conf 97%

A study of 29 stillbirth fetuses with renal agenesis identified a heterozygous RET mutation in 7/19 (37%) of those with

Een bron meldt “37%” in de context van nieren en urineleider: “A study of 29 stillbirth fetuses with renal agenesis identified a heterozygous RET mutation in 7/19 (37%) of those with BRA and in 2/10 (20%) of those with URA ( 31 ), ranking RET among the most frequent genes reported in BRA.”

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Frequentie / cijfer nieren en urineleider conf 97%

When fetal cases are included in future genetic invesigations of CAKUT, BRA will predictably be evaluated more often, as

Een bron meldt “2022 of 100” in de context van nieren en urineleider: “When fetal cases are included in future genetic invesigations of CAKUT, BRA will predictably be evaluated more often, as illustrated by a large series published in 2022 of 100 fetuses with severe renal defects was examined by targeted...

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Frequentie / cijfer Onderzoeksgrens conf 97%

1 , 2 In our cohort of 37 individuals with 17q12DS, a 30-35% and 40-65% had an increased frequency of atopic disorders a

Een bron meldt “37 individuals” in de context van algemeen: “1 , 2 In our cohort of 37 individuals with 17q12DS, a 30-35% and 40-65% had an increased frequency of atopic disorders and recurrent sinopulmonary infections, respectively, raising the possible immune dysregulation.”

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Frequentie / cijfer nieren en urineleider conf 97%

Keywords: duodenal obstruction, annular pancreas, ultrasound, prenatal diagnosis, chromosomal abnormality Abstract Backg

Een bron meldt “1 in 5000” in de context van diabetes en stofwisseling: “Keywords: duodenal obstruction, annular pancreas, ultrasound, prenatal diagnosis, chromosomal abnormality Abstract Background and Objectives : Congenital duodenal obstruction (CDO) is a very rare anomaly with an incidence of 1 in 5000-10,000...

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Frequentie / cijfer nieren en urineleider conf 97%

Thirty cases of CDO, in which both the diagnosis and ethiology were established, were categorized into two distinct grou

Een bron meldt “13 cases” in de context van diabetes en stofwisseling: “Thirty cases of CDO, in which both the diagnosis and ethiology were established, were categorized into two distinct groups based on their ethiology: CDO with annular pancreas (13 cases) and CDO without annular pancreas (17 cases).”

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Frequentie / cijfer nieren en urineleider conf 97%

Fetal growth restriction was identified in six cases (46.2%) with annular pancreas and five cases (29.4%) without annula

Een bron meldt “46.2%” in de context van diabetes en stofwisseling: “Fetal growth restriction was identified in six cases (46.2%) with annular pancreas and five cases (29.4%) without annular pancreas, with no significant difference between the groups.”

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Frequentie / cijfer nieren en urineleider conf 97%

Sixty-nine of the 74 individuals with diabetes and a T1D polygenic score exceeding an externally validated cutoff for di

Een bron meldt “74 individuals” in de context van diabetes en stofwisseling: “Sixty-nine of the 74 individuals with diabetes and a T1D polygenic score exceeding an externally validated cutoff for distinguishing T1D from not-T1D were confirmed to have T1D.”

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Frequentie / cijfer nieren en urineleider conf 97%

Of those 5 individuals with scores above the optimal cutoff without a diagnosis of T1D, there was one individual with CF

Een bron meldt “5 individuals” in de context van diabetes en stofwisseling: “Of those 5 individuals with scores above the optimal cutoff without a diagnosis of T1D, there was one individual with CFRD, two individuals with T2D, one individual with SIH, and one individual with diabetes in association with...

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Frequentie / cijfer nieren en urineleider conf 97%

Unlike other monogenic diabetes, about half of MODY5 cases are associated with a 17q12 deletion spanning approximately 1

Een bron meldt “5 cases” in de context van diabetes en stofwisseling: “Unlike other monogenic diabetes, about half of MODY5 cases are associated with a 17q12 deletion spanning approximately 1.5 Mb with variations from case to case encompassing 15 genes on average [ 4 , 5 ], including HNF1B [ 6 ], which explains the...

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Frequentie / cijfer Klachten & kenmerken conf 97%

Methods We examined prevalence rates of obesity and MetS in 103 adults with a typical 22q11.2 deletion (45.2% male, at m

Een bron meldt “45.2%” in de context van groei, darmen en voeding: “Methods We examined prevalence rates of obesity and MetS in 103 adults with a typical 22q11.2 deletion (45.2% male, at median age 30.0 (range 17-71) years) and compared these rates with population-based data.”

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Frequentie / cijfer Klachten & kenmerken conf 97%

Results Prevalence rates of generalized obesity (32.0%), abdominal obesity (51.5%), and MetS (33.0%) were significantly

Een bron meldt “32.0%” in de context van groei, darmen en voeding: “Results Prevalence rates of generalized obesity (32.0%), abdominal obesity (51.5%), and MetS (33.0%) were significantly higher compared to a population-based cohort (15.7% ( P < 0.0001), 36.1% ( P = 0.002), and 15.2% ( P < 0.0001), respectively).”

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Frequentie / cijfer Klachten & kenmerken conf 97%

Two previous single-center cohort studies in adults with 22q11.2DS reported high prevalence rates of generalized obesity

Een bron meldt “43.5%” in de context van groei, darmen en voeding: “Two previous single-center cohort studies in adults with 22q11.2DS reported high prevalence rates of generalized obesity (43.5%; 90/202 Canadians and 38.5%; 20/52 Belgian, respectively), based on body mass index (BMI) [ 7 , 8 ], the most widely...

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Frequentie / cijfer leren, taal en gedrag conf 97%

The most common reasons for referral were periodic 22q11.2DS-related assessments and health monitoring ( n = 63, 61.2%;

Een bron meldt “61.2%” in de context van leren, taal en gedrag: “The most common reasons for referral were periodic 22q11.2DS-related assessments and health monitoring ( n = 63, 61.2%; including transition to adult care), and psychiatric symptoms and/or psychosocial problems ( n = 23, 22.3%).”

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Frequentie / cijfer Klachten & kenmerken conf 97%

Comparison with prevalence rates of obesity and metabolic syndrome in the general population To compare prevalence rates

Een bron meldt “60%” in de context van groei, darmen en voeding: “Comparison with prevalence rates of obesity and metabolic syndrome in the general population To compare prevalence rates of obesity and MetS in the 22q11.2DS cohort with those in the general population, we used published data from Lifelines, a large...

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Frequentie / cijfer Klachten & kenmerken conf 97%

In contrast, the primary rick factor for CCA in Northeast Thailand particularly in Khon Kaen is liver fluke infection (

Een bron meldt “89%” in de context van lever en galblaas: “In contrast, the primary rick factor for CCA in Northeast Thailand particularly in Khon Kaen is liver fluke infection ( Opisthorchis Viverrini ), which accounts for approximately 89% of all liver cancers in this region [ 5 ].”

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Tegenstrijdig bewijs Onderzoeksgrens conf 97%

Let op: Overall, 17q12-related HNF1B whole gene deletions were the predominant type in our HNF1B pathogenic variant sp…

Een bron rapporteert geen verband of een negatieve bevinding: “Overall, 17q12-related HNF1B whole gene deletions were the predominant type in our HNF1B pathogenic variant spectrum, with no significant difference in the proportion of inherited versus de novo pathogenic variants ( p = 0.198).”

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Tegenstrijdig bewijs nieren en urineleider conf 97%

Let op: Because EA has already been identified in patients with 17q12 duplication or HNF1B point mutation, we screened…

Een bron rapporteert geen verband of een negatieve bevinding: “Because EA has already been identified in patients with 17q12 duplication or HNF1B point mutation, we screened HNF1B (QMPSF and direct sequencing) in nine additional patients with EA and renal abnormalities but failed to identify any pathogenic variant.”

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Tegenstrijdig bewijs nieren en urineleider conf 97%

Let op: In our case, there was no evidence of hepatic enlargement or fibrosis on fetal imaging, and the family history…

Een bron rapporteert geen verband of een negatieve bevinding: “In our case, there was no evidence of hepatic enlargement or fibrosis on fetal imaging, and the family history (maternal renal cyst and paternal diabetes) was more suggestive of an HNF1B -related disorder.”

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Nieuwe publicatie Genen & overerving conf 97%

Identification and functional analysis of a novel SMARCC2 splicing variant in a family with syndromic neurodevelopmental disorder

Background To determine the pathogenicity of a novel splicing variant in the SMARCC2 gene identified from a pair of adult male monozygotic twins with neurodevelopmental disorder, and to investigate the genotype-phenotype characteristics associated with SMARCC2 variants.

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Nieuwe publicatie nieren en urineleider conf 97%

Case-based learning: a case of maturity-onset diabetes of the young 5 (MODY5) due to 17q12 microdeletion with a diminished plasma glucagon level

Maturity-onset diabetes of the young type 5 (MODY5), causally associated with loss-of-function of the HNF1B gene, is a rare form of monogenic diabetes that has been underdiagnosed in part because microdeletions of chromosome 17q12 encompassing the HNF1B gene cannot be detected by sequencing-based approaches, which...

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