نتایج جستجو برای: congenital variations

تعداد نتایج: 305990  

2015
Uma Garg Anshul Singla

Congenital aural atresia, a rare entity, may be accompanied with variations in course of facial nerve and congenital cholesteatoma. In the present study, we describe three distinct cases of aural atresia, with successful management, according to the extent of atresia. Management of atresia is essentially a team work, comprising of otologist, plastic surgeon, radiologist and paediatrician, thus ...

Journal: :Attention, perception & psychophysics 2010
Micha Pfeuty Isabelle Peretz

Congenital amusia, characterized by a severe problem in detecting anomalies in melodies, is a lifelong disorder that has been ascribed to an acoustical pitch deficit. In the present study, we investigated how the perception of a duration is altered when it is bounded by tones varying in pitch. The results show that temporal accuracy is impaired by pitch variations as small as a quarter of a sem...

Journal: :Indian Journal of Case Reports 2023

Dextrocardia with situs inversus is a rare heart condition genetic predisposition. Although most individuals lead normal healthy life and usually, it an incidental finding. Due to their unique anatomical variations associated congenital variations, they may pose challenges attending clinicians. We are hereby reporting successful anesthetic management of the case 2.5-year-old child who presented...

Journal: :International Journal Of Medical Science And Clinical Invention 2022

Congenital anomalies and variations should be kept in mind when evaluating diseases the pediatric patient group. A 12 years old girl presented with findings of acut abdomen. Clinical laboratory data were consistent acute pancreatitis. Imaging showed a peristaltic cystic tissue thick wall central lumen head pancreas. In operation, it was shown that this lesion associated accessory pancreatic duc...

Journal: :Genetics and molecular research : GMR 2014
X Cao X M Zhou R Gan L Q Jiang L Lu Y Wang N Fan Y Yin N H Yan W H Yu X Y Liu

Genetic variations within the paired box gene 6 (PAX6) gene are associated with congenital aniridia. To detect the genetic defects in a Chinese twin family with congenital aniridia and nystagmus, exons of PAX6 were amplified by polymerase chain reaction (PCR), sequenced and compared with a reference database. Six members from the family of three generations were included in the study. The twins...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید