TY - CHAP M1 - Book, Section TI - Mohr Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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). SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164079032 ER -