Neurofaciodigitorenal syndrome

Neurofaciodigitorenal syndrome is a rare, multiple developmental anomalies syndrome characterized by neurological abnormalities (including megalencephaly, hypotonia, intellectual disability, abnormal EEG), dysmorphic facial features (high prominent forehead, grooved nasal tip, ptosis, ear anomalies) and acrorenal defects (such as triphalangism, broad halluces, unilateral renal agenesis). Additionally, intrauterine growth restriction, short stature and congenital heart defects may be associated. There have been no further descriptions in the literature since 1997.

Also known as: Freire Maia-Pinheiro-Opitz syndrome, neurofaciodigitorenal syndrome, Freire-Maia Pinheiro Opitz syndrome, Nfdr syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Neurofaciodigitorenal syndrome itself.