Results 141 to 150 of about 818 (182)

Cognitive Abilities and Lipomyelomeningocele

open access: yesPsychological Reports, 1993
Ten children with lipomyelomeningocele were evaluated with the WISC—R, the Wide Range Achievement Test—Revised, the Developmental Test of Visual-motor Integration, and the Child Behavior Checklist. These children were consecutive referrals to a birth defects clinic.
W N, Friedrich   +2 more
openaire   +3 more sources
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Adult cervicothoracic lipomyelomeningocele

Journal of Clinical Neuroscience, 2016
Lipomyelomeningocele (LMM) as a cause of tethered cord syndrome (TCS) commonly presents in childhood in the lumbosacral spine. Patients frequently present with cutaneous manifestations, progressive neurological deterioration, bladder dysfunction, and intractable pain. Early surgical intervention with untethering is recommended for symptomatic patients.
Nancy Abu-Bonsrah   +2 more
exaly   +3 more sources

An accessory limb with lipomyelomeningocele in a male

Pediatric Surgery International, 2013
At 7 months, an infant born with a third limb attached to a lumbosacral mass with an associated lipomyelomeningocele underwent removal of the limb and spinal cord detethering. Depending on the complexity of the pathology and proximity of the limb to viscera, consultation with neurosurgical and surgical colleagues is recommended.
Robert F Murphy   +2 more
exaly   +3 more sources

Lipomyelomeningocele

open access: yes, 2019
Lipomyelomeningocele (LMMC) is a form of spinal dysraphism involving a lipomatous malformation of the distal spinal cord. Physical examination may reveal cutaneous markers such as subcutaneous fat pads, asymmetric gluteal cleft, atypical dimples, hemangiomas, or atretic tails.
Christina Sayama
openaire   +2 more sources

Familial lipomyelomeningocele: A further report

open access: yesAmerican Journal of Medical Genetics Part A, 2004
AbstractLipomyelomeningocele is a form of spina bifida occulta with a distinct pathogenesis that differentiates it from open neural tube defects. Familial forms are rare and the condition may be polygenic. We report on 2 affected siblings with similar lesions and raise the possibility of an autosomal recessive pattern of inheritance with implications ...
Peter, Kannu   +2 more
openaire   +3 more sources

Surgical treatment for lipomyelomeningocele in children

open access: yesWorld Journal of Pediatrics, 2010
Lipomyelomeningocele (LMM) is a common and severe closed neural tube defect in children. Because of the complex anatomy of LMM and the difficulty in assessing the value of surgery, the management of patients with LMM is controversial. This study was undertaken to evaluate effective techniques and procedures in surgical treatment of LMM and to assess ...
Sheng-Li, Huang, Wei, Shi, Li-Gen, Zhang
openaire   +3 more sources

Bladder Function in Patients with Lipomyelomeningocele

open access: yesJournal of Urology, 1990
We evaluated preoperative and postoperative bladder function in 31 consecutive patients who underwent definitive operative correction of lipomyelomeningocele. Of 12 patients less than 1.5 years old at operation, bladder function was normal preoperatively and postoperatively in 5 (42%) and normalized postoperatively in 4 (33%).
L S, Foster   +3 more
openaire   +3 more sources

Lipomyelomeningocele

open access: yes, 2011
Sharad Rajpal, Bermans J. Iskandar
openaire   +2 more sources

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