New Orphanet summary reviewed by ITHACA : Hypertelorism, Teebi type

Hypertelorism, Teebi Type is a rare autosomal dominant malformation syndrome characterized by hypertelorism, omphalocoele, cleft lip, ear pits, uterine malformation (bicornuate uterus), and more variably by diaphragmatic hernia and congenital heart defects.

The summary has just been updated on Orphanet (ORPHA:1519) – October 2020 and revised by Pr Alain Verloes for ERN ITHACA.

Follow the link to read the summary