1.Prenatal diagnosis and genetic analysis of two fetuses with paternally derived 17q12 microdeletions.
Yuxin ZHANG ; Yingwen LIU ; Lulu YAN ; Danyan ZHUANG ; Haibo LI
Chinese Journal of Medical Genetics 2021;38(3):224-227
OBJECTIVE:
To reported on two fetuses diagnosed with 17q12 microdeletion syndrome.
METHODS:
The two fetuses were respectively found to have renal abnormalities and polyhydramnios upon second and third trimester ultrasonography. Umbilical cord blood of the first fetus and amniotic fluid of the second fetus were subjected to single nucleotide polymorphism array (SNP-array) analysis. After 17q12 microdeletion was found in the first fetus, SNP-array was carried out on peripheral blood samples of the parents to determine its origin. With the medical history of the parents taken into consideration, the father underwent high-throughput sequencing for 565 urinary system-related genes to exclude pathogenic or likely pathogenic variants associated with congenital malformations of the urinary and reproductive systems.
RESULTS:
In both fetuses, SNP-array has revealed a 1.42 Mb deletion at 17q12, or arr[hg19]17q12 (34 822 465-36 243 365) × 1. In both cases the microdeletion was inherited from the father, in whom no urinary disease-related pathogenic or likely pathogenic variants was identified.
CONCLUSION
Paternally derived 17q12 microdeletions probably underlay the genetic etiology of the two fetuses with renal ultrasound abnormalities and polyhydramnios. SNP-array can enable the diagnosis and facilitate genetic counseling and prenatal diagnosis for the families.
Chromosome Deletion
;
Chromosome Disorders
;
Chromosomes, Human, Pair 17
;
Female
;
Fetus
;
Genetic Counseling
;
Genetic Testing
;
Humans
;
Polyhydramnios/genetics*
;
Pregnancy
;
Prenatal Diagnosis
2.Recombinant Chromosome 4 with Partial 4p Deletion and 4q Duplication Inherited from Paternal Pericentric Inversion.
Se Jin MUN ; Eun Hae CHO ; Myoung Jae CHEY ; Gyu Hong SHIM ; Bo Moon SHIN ; Rae Kyung LEE ; Ji Kyung KO ; Soo Jin YOO
The Korean Journal of Laboratory Medicine 2010;30(1):89-92
Pericentric inversion of chromosome 4 can give rise to 2 alternate recombinant (rec) chromosomesby duplication or deletion of 4p. The deletion of distal 4p manifests as Wolf-Hirschhorn syndrome (WHS). Here, we report the molecular cytogenetic findings and clinical manifestations observed in an infant with 46,XX,rec(4)dup(4q)inv(4)(p16q31.3)pat. The infant was delivered by Cesarean section at the 33rd week of gestation because pleural effusion and polyhydramnios were detected on ultrasonography. At birth, the infant showed no malformation or dysfunction, except for a preauricular skin tag. Array comparative genomic hybridization analysis of neonatal peripheral blood samples showed a gain of 38 Mb on 4q31.3-qter and a loss of 3 Mb on 4p16.3, and these results were consistent with WHS. At the last follow-up at 8 months of age (corrected age, 6 months), the infant had not achieved complete head control.
*Chromosome Deletion
;
*Chromosome Duplication
;
*Chromosome Inversion
;
*Chromosomes, Human, Pair 4
;
Comparative Genomic Hybridization
;
Female
;
Gestational Age
;
Humans
;
Infant
;
Pleural Effusion/ultrasonography
;
Polyhydramnios/ultrasonography
;
Pregnancy
;
Wolf-Hirschhorn Syndrome/*genetics