17 research outputs found
SNP array typing provides new insights in chromosomal nondisjunction
Background Maternal uniparental disomy (UPD) of chromosome 7 (upd(7)mat)
accounts for approximately 10% of patients with Silver-Russell syndrome (SRS).
For upd(7)mat and trisomy 7, a significant number of mechanisms have been
proposed to explain the postzygotic formation of these chromosomal
compositions, but all have been based on as small number of cases. To obtain
the ratio of isodisomy and heterodisomy in UPDs (hUPD, iUPD) and to determine
the underlying formation mechanisms, we analysed a large cohort of upd(7)mat
patients (n = 73) by SNP array typing. Based on these data, we discuss the
UPDs and their underlying trisomy 7 formation mechanisms. Results A whole
chromosome 7 maternal iUPD was confirmed in 28.8%, a mixture or complete
maternal hUPD in 71.2% of patients. Conclusions We could demonstrate that
nondisjunction mechanism affecting chromosome 7 are similar to that of the
chromosomes more frequently involved in trisomy (and/or UPD), and that
mechanisms other than trisomic rescue have a lower significance than
previously suspected. Furthermore, we suggest SNP array typing for future
parent- and cell-stage-of origin studies in human aneuploidies as they allow
the definite classification of trisomies and UPDs, and provide information on
recombinational events and their suggested association with aneuploidy
formation
Profil psychologique et comportemental d’adultes atteints d’un syndrome de Silver-Russell.
International audienc
Cognitive and psychosocial profile in Silver-Russell syndrome: a first study in adults.
International audienc
Low Maternal DLK1 Levels at 26 Weeks Is Associated With Small for Gestational Age at Birth
International audienceDetecting SGA (small for gestational age) during pregnancy improves the fetal and neonatal prognosis. To date, there is no valid antenatal biomarker of SGA used in clinical practice. Maternal circulating DLK1 (delta-like non-canonical notch ligand 1) levels have been shown to be significantly lower in pregnant women at 36 weeks of gestation (WG) who delivered a SGA newborn than in controls. Data in the literature are contradictory on the association between maternal circulating DLK1 levels and placental vascular dysfunction. The objective was to determine if maternal DLK1 levels in the second trimester of pregnancy are predictive of SGA, and to assess whether the measurement of DLK1 levels in maternal blood could be a means to distinguish SGA with placental vascular dysfunction from that due to other causes. We conducted a nested cased-control study within the EDEN mother-child cohort. 193 SGA (birth weight < 10 th percentile) and 370 mother-child control (birth weight between the 25 th and 75 th percentile) matched pairs were identified in the EDEN cohort. Maternal circulating DLK1 levels at 26 WG were significantly lower for children born SGA than for controls (27.7 ± 8.7 ng/mL vs 30.4 ± 10.6 ng/mL, p = 0.001). Maternal blood DLK1 levels in the first quartile (DLK1 < 22.85 ng/mL) were associated with an odds ratio for SGA of 1.98 [1.15 - 3.37]. DLK1 was less predictive of SGA than ultrasound, with an area under the curve of 0.578. Maternal circulating DLK1 levels were not significantly different in cases of SGA with signs of placental vascular dysfunction (n = 63, 27.1 ± 9.2 ng/mL) than in those without placental dysfunction (n = 129, 28.0 ± 8.5 ng/mL, p = 0.53). The level of circulating DLK1 is reduced in the second trimester of pregnancy in cases of SGA at birth, independently of signs of placental vascular dysfunction. However, DLK1 alone cannot predict the risk of SGA
Cognitive profile in Silver-Russell syndrome: a first French study in adults.
International audienc
Profil cognitif dans le syndrome de Silver-Russell : une première étude française chez les adultes.
International audienc
Cognitive profile in Silver-Russell syndrome: a first French study in adults.
International audienc
Silver Russell syndrome in a preterm girl with 8q12.1 deletion encompassing PLAG1
Silver Russell syndrome (SRS) is a congenital disorder characterized by intrauterine growth retardation (IUGR), feeding difficulties and postnatal growth retardation. In a small number of cases, PLAG1 variants have been described (OMIM #618907). PLAG1 haploinsufficiency decreases Insulin-like growth factor 2 expression and produces a Silver Russell syndrome-like phenotype. Here, we describe the phenotype and molecular features of a 26 months girl with clinical features of SRS, and a de novo 2.1 Mb deletion encompassing PLAG1 is reported in association with clinical features suggestive of SRS.</p
11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome
International audienceThe 11p15 region harbors the IGF2/H19 imprinted domain, implicated in fetal and postnatal growth. Silver-Russell syndrome (SRS) is characterized by fetal and postnatal growth failure, and is caused principally by hypomethylation of the 11p15 imprinting control region 1 (ICR1). However, the mechanisms leading to ICR1 hypomethylation remain unknown. Maternally inherited genetic defects affecting the ICR1 domain have been associated with ICR1 hypermethylation and Beckwith-Wiedemann syndrome (an overgrowth syndrome, the clinical and molecular mirror of SRS), and paternal deletions of IGF2 enhancers have been detected in four SRS patients. However, no paternal deletions of ICR1 have ever been associated with hypomethylation of the IGF2/H19 domain in SRS. We screened for new genetic defects within the ICR1 in a cohort of 234 SRS patients with hypomethylated IGF2/H19 domain. We report deletions close to the boundaries of ICR1 on the paternal allele in one familial and two sporadic cases of SRS with ICR1 hypomethylation. These deletions are associated with hypomethylation of the remaining CBS, and decreased IGF2 expression. These results suggest that these regions are most likely required to maintain methylation after fertilization. We estimate these anomalies to occur in about 1% of SRS cases with ICR1 hypomethylation