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About 355 results

ALLMedicine™ Treacher Collins Syndrome Center

Research & Reviews  134 results

Mandibulofacial Dysostosis (Treacher Collins Syndrome)
https://emedicine.medscape.com/article/946143-print

Jan 20th, 2023 - Practice Essentials Mandibulofacial dysostosis,[1] also known as Treacher Collins syndrome (TCS; entry 154500 in the Online Mendelian Inheritance in Man [OMIM] classification system), is an inherited developmental disorder with a prevalence estima...

Mandibulofacial Dysostosis (Treacher Collins Syndrome)
https://emedicine.medscape.com/article/946143-overview

Jan 20th, 2023 - Practice Essentials Mandibulofacial dysostosis, [1] also known as Treacher Collins syndrome (TCS; entry 154500 in the Online Mendelian Inheritance in Man [OMIM] classification system), is an inherited developmental disorder with a prevalence estim...

Mandibulofacial Dysostosis (Treacher Collins Syndrome)
http://emedicine.medscape.com/article/946143-overview

Jan 20th, 2023 - Practice Essentials Mandibulofacial dysostosis, [1] also known as Treacher Collins syndrome (TCS; entry 154500 in the Online Mendelian Inheritance in Man [OMIM] classification system), is an inherited developmental disorder with a prevalence estim...

Bite Force, Masticatory Performance, and Nutritional Status of Adult Individuals With T...
https://doi.org/10.1177/10556656221132376
The Cleft Palate-craniofacial Journal : Official Publicat... Medeiros LH, de Barros SP et. al.

Dec 23rd, 2022 - To characterize the stomatognathic system of individuals with Treacher Collins syndrome (TCS) by assessing bite force (BF) and masticatory performance (MP) and to evaluate the nutritional status (NS) of this population through anthropometric measu...

A systematic review on Treacher Collins syndrome: Correlation between molecular genetic...
https://doi.org/10.1111/cge.14243
Clinical Genetics; Ulhaq ZS, Nurputra DK et. al.

Oct 8th, 2022 - Treacher Collins syndrome (TCS, OMIM: 154500) is a rare congenital craniofacial disorder that is caused by variants in the genes TCOF1, POLR1D, POLR1C, and POLR1B. Studies on the association between phenotypic variability and their relative varian...

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Clinicaltrials.gov  2 results

Suitable Method for Routine Diagnostics of EER in Children With Otitis Media With Effusion
https://clinicaltrials.gov/ct2/show/NCT02183974

Jul 8th, 2014 - Children at the age between 1 to 7 years diagnosed with bilateral or unilateral OME who underwent adenoidectomy and myringotomy with insertion of ventilation tube were included in the prospective study. OME was defined as effusion in the middle ea...

Three Methods Used in the Diagnosis of EER in Children With OME
https://clinicaltrials.gov/ct2/show/NCT02183961

Jul 8th, 2014 - Children aged between 1 and 7 years diagnosed with bilateral or unilateral OME who underwent adenoidectomy and myringotomy with insertion of a ventilation tube were included in the prospective study. OME was defined as effusion in the middle ear b...

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News  2 results

Physician Education, Precision Medicine, Translational Science and Repurposing Drugs to Be Among Topics at NORD Summit
https://www.mdedge.com/clinicalneurologynews/article/102622/physician-education-precision-medicine-translational-science

Sep 14th, 2015 - Christopher Austin, MD, Director of the National Center for Advancing Translational Sciences (NCATS) will deliver the keynote luncheon address on the first day of the National Organization for Rare Disorders (NORD) Rare Diseases and Orphan Product.

Physician Education, Precision Medicine, Translational Science and Repurposing Drugs to Be Among Topics at NORD Summit
https://www.mdedge.com/clinicianreviews/article/102825/physician-education-precision-medicine-translational-science-and

Sep 14th, 2015 - Christopher Austin, MD, Director of the National Center for Advancing Translational Sciences (NCATS) will deliver the keynote luncheon address on the first day of the National Organization for Rare Disorders (NORD) Rare Diseases and Orphan Product.

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Patient Education  4 results see all →