Prenatal diagnosis and postnatal follow-up of a child with mosaic trisomy 22 with several levels of mosaicism in different tissues
Author:
Publisher
Wiley
Subject
Obstetrics and Gynaecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1447-0756.2010.01278.x/fullpdf
Reference11 articles.
1. Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization;Wolstenholme;Prenat Diagn,1996
2. Incomplete trisomy 22. III. Mosaic-trisomy 22 and the problem of full trisomy 22;Schinzel;Hum Genet,1981
3. A second case of intrauterine growth retardation and primary hypospadias associated with a trisomy 22 placenta but with biparental inheritance of chromosome 22 in the fetus;Bryan;Prenat Diagn,2002
4. Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood sampling;Berghella;Prenat Diagn,1998
5. Prenatally diagnosed mosaic trisomy 22 in a fetus with left ventricular non-compaction cardiomyopathy;Wang;Am J Med Genet A,2007
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2. Occurrence of mosaic trisomy 22 and pericentric inversion of chromosome 9 in a patient with a good prognosis;BMC Medical Genomics;2023-11-13
3. Trisomy 22: First and Second Trimester Cytogenetic Analysis and Phenotypic Presentation in a Series of Seven Cases;Fetal Diagnosis and Therapy;2023-11-03
4. Pregnancy outcome of confined placental mosaicism: meta-analysis of cohort studies;American Journal of Obstetrics and Gynecology;2022-11
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