[Observation of a fully developed non-familial cranio-digito-facial anomaly; association of Crouzon's & Alpert's syndromes].
D003394:Craniofacial Dysostosis; D003398:Craniosynostoses; D005385:Fingers / Q000002:abnormalities*; D006801:Humans; D006972:Hypertelorism / Q000150:complications*; D013577:Syndrome
ACROCEPHALY; FINGERS/abnormalities; HYPERTELORISM/complications
Beobachtung elner nichtfamiliären, voll ausgebildeten kranio-digito-facialen Anomalie; Kombination der Syndrome Crouzon und Apert.