Results 101 to 110 of about 1,422,626 (192)

Treacher Collins syndrome – report of two cases

open access: yes, 1987
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
core  

Treacher-Collins syndrome.

open access: yesJBR-BTR : organe de la Societe royale belge de radiologie (SRBR) = orgaan van de Koninklijke Belgische Vereniging voor Radiologie (KBVR), 2006
Geniets, C.   +4 more
  +6 more sources

TREACHER COLLINS SYNDROME WITH ASSOCIATION OF HYPOSPADIA: REPORT OF A CASE

open access: yes, 1981
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
core  

Basic reading skills : a case study of an adult with Treacher Collins Syndrome / Lilly S. Kulanthai. [PDF]

open access: yes, 2012
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]

open access: yes, 2009
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
core  

Treacher Collins Syndrome in Siblings - A Case Report

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2007
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

open access: yes, 2019
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
core  

Considerations in Eyelid Reconstruction in Treacher Collins Syndrome: A Scoping Review. [PDF]

open access: yesFACE (Thousand Oaks), 2023
Vandevender J   +4 more
europepmc   +1 more source

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