The deletion 9p syndrome is a well-recognized entity, with about 100 reported cases. Characteristic findings include trigonocephaly, upslanting palpebral fissures, epicanthal folds, anteverted nares, long philtrum, posteriorly angulated and poorly formed ears, excess of whorls on the fingers, and me
A case of 9p- syndrome
β Scribed by Yoshikazu Kuroki; Shunpei Yokota; Hiroshi Nakai; Yoshifumi Yamamoto; Ichiro Matsui
- Publisher
- Springer
- Year
- 1977
- Tongue
- English
- Weight
- 250 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0340-6717
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β¦ Synopsis
An 8-month-old female child with the 9p- karyotype: 46,XX,del(9) (p22) is presented, being the first case from among Oriental people. She has many clinical features similar to those described in Caucasian cases.
π SIMILAR VOLUMES
A low-birth-weight near-term male infant was found to have a non-familial 47,XΒ₯ chromosome complement with an extra medimn-sized metacentrie chromosome slightly larger than a number 16. By Giemsa-trypsin (G-banding) this extra chromosome was determined to be a number 9 with deletion of approximately
A 5-year-old boy with multiple minor anomalies and mental retardation was found to have chromosomal condition of 46,XY,inv dup(9p) (pter leads to p13::p21 leads to p24::p13 leads to qter). The clinical features of the propositus fit well with those of trisomy 9p which have been established to be a c