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PMID: 2118776 Published · ppublish English Journal Article

Rubinstein-Taybi syndrome: the changing face.

American journal of medical genetics. Supplement ·Vol. 6 ·1990-00-00 ·Pages 38-41

Allanson JE

Abstract

Rubinstein-Taybi syndrome is a rare multiple congenital anomaly (MCA) syndrome comprising mental and growth retardation, broad thumbs and big toes, and unusual face. The classical appearance is easy to recognize. It includes downslant of the palpebral fissures, epicanthal folds, ptosis, strabismus, highly arched palate, and apparently low-set angulated ears with thickened helices. The nose has a beaked appearance, broad fleshy bridge, deviated septum that is long, protruding below the level of the nasal alae with an associated short columella. Since the typical facial phenotype may not be obvious until late childhood, I have evaluated more than 40 cases of Rubinstein-Taybi syndrome, seen at varying ages from the newborn period through infancy, childhood, and adulthood, in order to learn more about the early facial appearance.

MeSH Terms
Abnormalities, Multiple/pathology Adolescent Adult Child Child, Preschool Face/pathology Humans Infant Rubinstein-Taybi Syndrome/pathology
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Allanson J E
Division of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada.
Article Info
Journal
American journal of medical genetics. Supplement
Abbr.
Am J Med Genet Suppl
ISSN
1040-3787
Published
1990-00-00
Pages
38-41
Language
English
Region
United States
NLM ID
8706133
Subset
IM
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