Carey-Fineman-Ziter syndrome 1

A rare condition characterized by the association of hypotonia, Moebius sequence (bilateral congenital facial palsy with impairment of ocular abduction), Pierre-Robin sequence (micrognathia, glossoptosis, and high-arched or cleft palate), unusual face, and growth delay.

Also known as: CFZS1, Carey-Fineman-Ziter syndrome 1, myopathy, congenital nonprogressive, with Moebius sequence and Robin sequence, myopathy-Moebius-Robin syndrome, CFZS, Carey Fineman Ziter syndrome, Moebius sequence, Robin complex, and hypotonia, congenital nonprogressive myopathy with Moebius and Robin sequences

0 clinical trials for this condition and its sub-types, 0 tagged with Carey-Fineman-Ziter syndrome 1 itself.