RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164079032 T1 Mohr Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164079032 RD 2024/03/28 AB It is a very rare medical condition that is part of a spectrum of diseases called Oral-Facial-Digital Syndrome (OFDS). There are 10 disorders that have been identified in this condition and the Mohr Syndrome is Type II. It is characterized by a familial association of deafness with facial hypoplasia and minor midline cleft (tongue, lip, palate). Clinically, the symptoms include frequent episodic neuromuscular disturbances, coarse hair, grainy skin lesions, polycystic kidneys (after the age of 10 years), malformation of the hands and feet (eg, unilateral polysyndactyly), shortened limbs, and differing degrees of mental retardation. There are reports of an association with congenital cardiac defects (eg, tetralogy of Fallot).