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.
Comprehensive, easy-to-understand information about this condition
Checking for content...
acromegaloid facial appearance syndrome
MONDO:0007051
Hypoglossia-hypodactyly syndrome
MONDO:0007073
Brachymorphism-onychodysplasia-dysphalangism syndrome
MONDO:0007230
campomelic dysplasia
MONDO:0007251
cerebrocostomandibular syndrome
MONDO:0007301
autosomal dominant popliteal pterygium syndrome
MONDO:0007334