Results 11 to 20 of about 1,727 (229)
Lipomyelomeningocele: A Case Report [PDF]
: Introduction: Lipomyelomeningocele (LMMC) is a neural tube defect with neural elements incorporated into the spinal lipoma with the prevalence ranging from 0.3-0.6 per 10000 live births.
Vinay P Solabannavar, Vijetha Vikram
semanticscholar +3 more sources
Prenatally diagnosed fetal thoraco-lumbar spine duplication associated with lipomyelomeningocele: An extremely rare case of split cord malformation. [PDF]
Spine duplication is considered rare, a more serious form of split cord malformation. Ultrasonographic evaluation of the spine in the second trimester is central to the antenatal diagnosis of spinal malformations. Here, we report a case of thoraco-lumbar
Akalın M +3 more
europepmc +3 more sources
Background: Lipomyelomeningocele (LMMC), the most complex spinal lipoma and a common spinal malformation, can cause complications ranging from bladder dysfunction to significant neurological deficits.
Devansh Mishra +2 more
doaj +4 more sources
Cervical lipomyelomeningocele: case Illustration [PDF]
Cervical lipomyelomeningocele is a rare congenital spinal pathology. Lipomyelomeningocele is the commonest cause of congenital tethering, which causes neurological deterioration due to the conus medullaris and root ischemia. Early intervention is recommended even in cases with normal neurological examinations in order to prevent deterioration but our ...
Doğa Gürkanlar, Miizeyyen Gönül
+7 more sources
A Case Report of Lumbosacral Lipomyelomeningocele with Tethered Cord Syndrome
The objective is to describe a rare case of lumbosacral lipomyelomeningocele with Tethered Cord Syndrome. Tethered cord syndrome is a neurological disorder caused by tissue attachments that limit the movement of spinal cord within the spinal column.
Dr. Deepak Mewara +5 more
semanticscholar +3 more sources
Challenges in the management of caudal duplication syndrome [PDF]
Caudal duplication syndrome (CDS) is a rare developmental anomaly in which embryonic cloaca and notochord structures are duplicated [1]. Due to the diverse clinical manifestation and rarity of CDS, it is crucial to report every case and to share ...
Laine Bekere +3 more
doaj +3 more sources
Anomalous osseous limb: A sneak peek into rare association with lipomyelomeningocele – A case report
Anomalous osseous limb is a rare entity and its association with spinal dysraphism is all the more rarer. We report one such case of lipomyelomeningocele in 1-month-old female, with associated anomalous osseous structure/ limb in relation to iliac bones.
Laxamikant Dogra +3 more
semanticscholar +3 more sources
Identical twins with lumbosacral lipomyelomeningocele [PDF]
Lipomyelomeningocele, a congenital spine defect, is presented as skin-covered lipomatous tissue that attaches to the cord in different ways according to its subtypes. Unlike other types of neural tube defects, the exact cause of this birth defect has not been confirmed yet, but it is proposed to be a multifactorial disease with involvement of both ...
Sara Hanaei +5 more
openalex +3 more sources
Cartilage within lipomyelomeningocele and ulnar longitudinal deficiency syndrome as VACTERL association, alliance in SHH/GLI3, and Wnt pathway: illustrative case. [PDF]
BACKGROUND Lipomyelomeningocele associated with an ulnar club hand in the spectrum of VACTERL association ([costo-]vertebral abnormalities; anal atresia; cardiac defects; tracheal-esophageal abnomalities, including atresia, stenosis, and fistula; renal ...
Shimekit MA +3 more
europepmc +2 more sources
Introduction: Lipomyelomeningocele is one of closed spinal dysraphism, inherently associated with tethered cord. Its prevalence ranges between 0.3 and 0.6 per 10.000 live births.
Yurima Indriyani +3 more
semanticscholar +3 more sources

