Results 101 to 110 of about 1,422,626 (192)
Treacher Collins syndrome – report of two cases
Two cases of Treacher Collins syndrome (Mandibulofacial dysostosis) are presented. No hematological, biochemical or immuno¬logical abnormalities were detected in these patients, nor structural or numerical chromosomal discrepancies.
Rajendran, R. +3 more
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Geniets, C. +4 more
+6 more sources
TREACHER COLLINS SYNDROME WITH ASSOCIATION OF HYPOSPADIA: REPORT OF A CASE
We report a 6-year-old boy of Treacher Collins syndrorne associated with penoscrotal hypospadias. The patient shows following feature that is typical of Treacher Collins syndrome: 1) Hypoplasia of the left malar bone.
西村, 真治 +5 more
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Basic reading skills : a case study of an adult with Treacher Collins Syndrome / Lilly S. Kulanthai. [PDF]
Everyone regardless of age and gender should be given an opportunity to learn, especially to read. Literacy improves lives of people in tremendous ways.
S. Kulanthai, Lilly
core
Orofacial features of Treacher Collins syndrome [PDF]
Treacher Collins syndrome (TCS) is a rare autosomal dominant disorder of craniofacial development. Major features include midface hypoplasia, micrognathia, microtia, conductive hearing loss, and cleft palate.
Bonan,Paulo Rogério Ferreti +5 more
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Treacher Collins Syndrome in Siblings - A Case Report
Treacher Collin′s syndrome is a rare syndrome that is characterized primarily by defects of the structures derived from first and second branchial arches.
K S Ganapathy +3 more
doaj
Disostosis mandibulofacial (síndrome de treacher collins). Reporte de un caso
La disostosis mandibulofacial o síndrome de TreacherCollins.es un rarotrastornocraneofacial congénito de herencia autosómica dominante. A pesar que su expresión fenotípica es muy variable, el diagnóstico es fundamentalmente clínico.
Piedra Bravo, Yadira Lucía +1 more
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Considerations in Eyelid Reconstruction in Treacher Collins Syndrome: A Scoping Review. [PDF]
Vandevender J +4 more
europepmc +1 more source

