Treacher Collins Syndrome In The Newborn
نویسنده
چکیده
a b c Dr. Girish Gopal , Dr. Divya Durga , Dr. S. Prashanth Senior Resident, Department of Pediatrics, Mysore Medical College and Research Institute, Mysore -570001, Karnataka. Post graduate student, Department of Pediatrics, Mysore Medical College and Research Institute, Mysore -570001, Karnataka. Assistant Professor, Department of Pediatrics, Mysore Medical College and Research Institute, Mysore -570001, Karnataka.
منابع مشابه
Treacher Collins Syndrome
Treacher Collins syndrome (TCS) is a genetic disease that alters the development of bones and other tissues in the face, and presents variable expressivity. At least three genes TCOF1, POLR1D, and POLR1C were recognized to be at the origin of this syndrome which may be inherited through either an autosomal dominant or autosomal recessive pattern. TCS changes can be divided into otological, opht...
متن کامل[Difficult fiberoptic tracheal intubation in 1 month-old infant with Treacher Collins Syndrome].
Neonates and small infants with craniofacial malformation may be very difficult or impossible to mask ventilate or intubate. We would like to report the fiberoptic intubation of a small infant with Treacher Collins Syndrome using the technique described by Ellis et al. CASE REPORT An one month-old infant with Treacher Collins Syndrome was scheduled for mandibular surgery under general endotra...
متن کاملManagement of obstructive sleep apnea in a Treacher Collins syndrome patient using distraction osteogenesis of the mandible
In this study, we present the surgical treatment of obstructive sleep apnea in a child with Treacher Collins syndrome. A 10-year-old girl with a past history of Treacher Collins syndrome presented to our clinic with her parents for respiratory distress and insomnia. The patient was referred to a sleep laboratory where she was diagnosed with obstructive sleep apnea, which was a consequence of he...
متن کاملResults of the implantation of bone-anchored hearing aids in patients with treacher-collins syndrome
INTRODUCTION Treacher-Collins syndrome is characterized by craniofacial malformations, narrowing of the external auditory canal (EAC), and, in 30% of cases, agenesis of the canal and ossicular chain defects. The use of hearing aids (HA) is not possible in cases in which agenesis or stenosis of the EAC accompanies conductive deafness. In contrast, bone conduction implants such as the Bone Ancho...
متن کاملTreacher Collins Syndrome associated with foot deformity and genital anomalies Ayak deformitesi ve genital anomali ile birliktelik gösteren Treacher Collins Sendromu
19 T reacher Collins syndrome is an autosomal dominant genetic disorder and affects mainly the head and face. The incidence is estimated to range from 1 in 40 000 to in 70 000 live births. The patients with TCS have usually characteristic bilateral facial anomalies (1). This article reports a case of Treacher Collins syndrome with the presence of genital anomalies and foot abnormality that has ...
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