Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Spinal Dysraphism: A Three Year Experience at Armed Forces Institute of Radiology and Imaging
by
Nisar, Uzma
, Iftikhar, Ammara
, Nisar, Shahana
, Halim, Aliya
, Nasir, Hina
, Slehria, Atiq Ur Rehman
in
Age
/ Armed Forces
/ Birth defects
/ Congenital diseases
/ Embryonic development
/ Females
/ Genetic disorders
/ Magnetic resonance imaging
/ Radiation
/ Scoliosis
/ Sinuses
/ Skin
/ Spina bifida
/ Vertebrae
2022
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Spinal Dysraphism: A Three Year Experience at Armed Forces Institute of Radiology and Imaging
by
Nisar, Uzma
, Iftikhar, Ammara
, Nisar, Shahana
, Halim, Aliya
, Nasir, Hina
, Slehria, Atiq Ur Rehman
in
Age
/ Armed Forces
/ Birth defects
/ Congenital diseases
/ Embryonic development
/ Females
/ Genetic disorders
/ Magnetic resonance imaging
/ Radiation
/ Scoliosis
/ Sinuses
/ Skin
/ Spina bifida
/ Vertebrae
2022
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Spinal Dysraphism: A Three Year Experience at Armed Forces Institute of Radiology and Imaging
by
Nisar, Uzma
, Iftikhar, Ammara
, Nisar, Shahana
, Halim, Aliya
, Nasir, Hina
, Slehria, Atiq Ur Rehman
in
Age
/ Armed Forces
/ Birth defects
/ Congenital diseases
/ Embryonic development
/ Females
/ Genetic disorders
/ Magnetic resonance imaging
/ Radiation
/ Scoliosis
/ Sinuses
/ Skin
/ Spina bifida
/ Vertebrae
2022
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Spinal Dysraphism: A Three Year Experience at Armed Forces Institute of Radiology and Imaging
Journal Article
Spinal Dysraphism: A Three Year Experience at Armed Forces Institute of Radiology and Imaging
2022
Request Book From Autostore
and Choose the Collection Method
Overview
Objective: To review all the patients of spinal dysraphism referred to our center over a three year period in order to identify the most typical neuro-radiological appearances on Magnetic Resonance Imaging. Study Design: Cross sectional study. Place and Duration of Study: Armed Forces Institute of Radiology and Imaging, Rawalpindi from Jan 2016 to Dec 2018. Methodology: MR spine reports of 144 patients of spinal dysraphism were retrospectively analyzed. Age, gender, indication for MRI, operative status, and neuro-radiological features (including site and type of lesion) were recorded for these patients. Results: Congenital spinal malformations were more frequent among females87 (60.4%) and between 0-20 years 135 (93.9%) of age. Tethered cord 97 (67.4%) was the most common congenital spinal abnormality followed by spina bifida, diastematomyelia, vertebral segmentation anomalies, myelomeningocele, menigocele. Lip-myelomeningocele, lipoma of filum terminale, and sacral agenesis. Frequently observed associated abnormalities included scoliosis 61 (42.4 %), syrinx 47 (32.6%) and dural ectasia 40 (27.8 %). Conclusion: Congenital spinal malformations are usually complex with variable radiological appearances. Modern high resolution MRI screening is the examination of choice for identification, preoperative evaluation, and long term follow up of such congenital anomalies.
Publisher
Knowledge Bylanes,Army Medical Corps
Subject
This website uses cookies to ensure you get the best experience on our website.