1p32-p31 deletion syndrome

1p32-p31 deletion syndrome Relevant markers:

Micrognathia/retrognathiaProminent foreheadComplete agenesis of corpus callosum

Parents markers:

Ambiguous genitaliaCorpus callosum hypoplasiaMacrocephalyVentriculomegaly

References:

2007	PLoS Genet	Case series (one prenatal)	Read on PubMed
2011	Taiwan J Obstet Gynecol	Case Report	Read on PubMed