Abstract
Twenty-two cases of terminal deletions of the long arm of chromosome 7 have been reported. We present 5 new cases, 3 of which were ascertained due to fetal holoprosencephaly, one due to anencephaly, and one due to multiple structural defects in a 15-year-old boy. The presence of holoprosencephaly in 3 of the 5 cases reported herein and in 2 previously reported cases suggests that this manifestation may be commonly observed in individuals with deletion 7q.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 53-55 |
| Number of pages | 3 |
| Journal | American journal of medical genetics |
| Volume | 36 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1990 |
Keywords
- holoprosencephaly
ASJC Scopus subject areas
- Genetics(clinical)