Frank–ter Haar syndrome—additional findings?

التفاصيل البيبلوغرافية
العنوان: Frank–ter Haar syndrome—additional findings?
المؤلفون: Cemil Işler, Nihan Aksakallı, İlknur Özcan, Ş. Neslihan Şenel, Tolga Sitilci, Taha Emre Köse
المصدر: Dentomaxillofacial Radiology. 45:20150119
بيانات النشر: British Institute of Radiology, 2016.
سنة النشر: 2016
مصطلحات موضوعية: Heart Defects, Congenital, Male, 0301 basic medicine, Sphenoid Sinus, Dentigerous Cyst, Craniofacial abnormality, Developmental Disabilities, Glaucoma, Case Report, Osteochondrodysplasias, Craniofacial Abnormalities, Young Adult, 03 medical and health sciences, Megalocornea, 0302 clinical medicine, Frank–ter Haar syndrome, Ethmoid Sinus, Radiography, Panoramic, Temporal bone, medicine, Humans, Radiology, Nuclear Medicine and imaging, General Dentistry, Wide anterior fontanel, business.industry, Mandibular Condyle, Tooth, Impacted, Temporal Bone, General Medicine, Anatomy, Cone-Beam Computed Tomography, Maxillary Sinus, medicine.disease, Molar, stomatognathic diseases, 030104 developmental biology, Otorhinolaryngology, business, human activities, Brachycephaly, Full cheeks, 030217 neurology & neurosurgery
الوصف: Frank–ter Haar syndrome is a genetic disease that is transmitted by autosomal recessive pattern with characteristic features such as megalocornea or glaucoma, a prominent coccyx, heart defects, developmental delays, brachycephaly, a wide anterior fontanel, finger flexion deformities, full cheeks and micrognathia. Dentomaxillofacial features of this syndrome are not well documented in the literature. We present of a 21-year-old male with Frank–ter Haar syndrome and some features that may be linked with this syndrome not reported before in the literature.
تدمد: 1476-542X
0250-832X
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8cb84fd3af5f50af2a707a2f3d03b56Test
https://doi.org/10.1259/dmfr.20150119Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....a8cb84fd3af5f50af2a707a2f3d03b56
قاعدة البيانات: OpenAIRE