An extremely rare autosomal recessive disorder with characteristics of bilateral facial palsy with masked facies, sensorineural hearing loss, dysmorphic features (midfacial retrusion, low-set ears) and strabismus.

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

congenitale erfelijke faciale paralyse, variabel gehoorverlies-syndroom

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Belongs to the group of multiple congenital anomalies/mental retardation syndromes with intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

syndroom van McDonough

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Compression facies

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

compressie van aangezicht

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]

Anderen hebben gezocht naar : compression facies corvisart complex corvisart facies cardiac facies prima facie evidence prima facie proof

datacenter (1): www.wordscope.be (v4.0.br)

'corvisart facies' ->

Date index: 2022-11-12