The 3p deletion syndrome is an unusual condition. The few cases described are mainly de novo. We described a familial case detected in a prenatal diagnosis. Three members of the family had the 3p26.3-p26.1 deletion; however, only the son presented clinical features.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077371 | PMC |
| http://dx.doi.org/10.1002/ccr3.4036 | DOI Listing |
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The 3p deletion syndrome is an unusual condition. The few cases described are mainly de novo. We described a familial case detected in a prenatal diagnosis.
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