branchiogenic deafness syndrome https://www.malacards.org/card/branchiogenic_deafness_syndrome_2 Branchiogenic deafness syndrome is a multiple congenital anomalies syndrome, described in one family to date, characterized by branchial cysts or fistulae; ear malformations; congenital hearing loss (conductive, sensorineural, and mixed); internal auditory canal hypoplasia; strabismus; trismus; abnormal fifth fingers; vitiliginous lesions, short stature; and mild learning disability. Renal and uretral abnormalities are absent. BRANCHIOGENIC-deafness syndrome Mégarbané-Loiselet syndrome MESH:C563780 SCTID:717944002 GARD:0016648 OMIM:609166 UMLS:C1836673 MC)garbanC)-Loiselet syndrome MONDO:0012209 MEDGEN:322970 Orphanet:50815 multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome