Postaxial acrofacial dysostosis or Miller syndrome. A case report. 1989

D Barbuti, and C Orazi, and A Reale, and C Paradisi
Department of Radiology, Ospedale Bambino Gesu, Roma, Italy.

A case of postaxial acrofacial dysostosis (Miller syndrome) is presented. This rare syndrome is essentially characterized by a Treacher-Collins-like facial appearance together with absence of the fifth digital ray of all limbs and variable forearm hypoplasia.

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D005145 Face The anterior portion of the head that includes the skin, muscles, and structures of the forehead, eyes, nose, mouth, cheeks, and jaw. Faces
D005385 Fingers Four or five slender jointed digits in humans and primates, attached to each HAND. Finger
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000015 Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. Multiple Abnormalities
D013577 Syndrome A characteristic symptom complex. Symptom Cluster,Cluster, Symptom,Clusters, Symptom,Symptom Clusters,Syndromes
D014034 Toes Any one of five terminal digits of the vertebrate FOOT. Toe

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