Skin manifestations in a case of trisomy 16 mosaicism
β Scribed by L.B. Ousager; F. Brandrup; C. Brasch-Andersen; A. Erlendsson
- Book ID
- 108668490
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 379 KB
- Volume
- 154
- Category
- Article
- ISSN
- 0007-0963
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## Abstract Postnatally ascertained trisomy 16 mosaicism is a rare diagnosis, with only three reported cases to date with no defined clinical phenotype. Trisomy 16 mosaicism diagnosed prenatally is common and associated with variable pregnancy outcomes ranging from stillbirth with multiple congenit
## Abstract Trisomy 16 mosaicism detected at midtrimester amniocentesis is rare and indicative of true fetal mosaicism. We report a case of mosaic trisomy 16 diagnosed by amniocentesis in which the sonographic findings included fetal pulmonary artery stenosis, a single umbilical artery, and early o
An 8-year-old male with mental retardation, speech difficulties, and minor congenital anomalies is presented. The clinical findings suggest the trisomy-8 syndrome. The karyotype indicates trisomy-8 mosaicism with trisomic as well as normal cell lines in blood lymphocytes.