Eight of the 22 patients had spina bifida aperta, and 14 had spina bifida occulta. These included eight cases with repaired myelomeningocele, seven with an intraspinal lipoma and tethering of cord , three with dermal sinuses, and one with diastematomyelia. Bulging and low signal intensity of the nucleus pulposus on T2-weighted images are the criteria for disk degeneration [1 , 2] . In our study...

INTRODUCTION Assuming that spina bifida (SB) is a genetically controlled disease, the aim of our study was to evaluate the degree of genetic homozygosity and the distribution of AB0 blood types among patients with SB occulta and SB aperta by the homozygously recessive characteristics (HRC) test. MATERIAL AND METHODS Our study included an analysis of the presence, distribution and individual c...

INTRODUCTION Lipomyelomeningocele is a form of the spina bifida occulta, which show differentiation from spina bifida aperta by pathogenesis. Laterally located thoracal lipomyelomeningocele is very rare congenital spinal pathology. The clinical presentation may be soft tissue mass, sensorial-motor loss and/or bladder dysfunction. CASE PRESENTATION Here we presented a 10-month-old girl patient...

Lorber, J. (1972). Archives of Disease in Childhood, 47, 854. Spina bifida cystica: results of treatment of 270 consecutive cases with criteria for selection for the future. The disappointing results of treatment in 270 consecutive unselected cases of spina bifida admitted during a 27-month period are detailed. Massive effort has led to much avoidable suffering at an exorbitant cost in manpower...

Meningitis is a well-known complication of meningomyelocele, but the problems of its diagnosis and treatment have so far received scant attention. Some children with meningomyelocele have a small neurological deficit and no hydrocephalus. Others with hydrocephalus may benefit from modern treatment and grow up to lead normal lives. The problem of meningitis in meningomyelocele is, therefore, wor...

589 T HIS STUDY iS conceriled with the family history of 722 infants who were horn with spina bifida cystica (meningomyelocele, myelocele and meningocele) and who were referred to the Children’s Hospital, Sheffield, for surgical treatment. No cases were excluded from this investigation. None of the infants or children were referred for genetic advice hecautse of special problems, and if there w...

Objectives-A case-control study was carried out to explore associations between spina bifida and occupational exposure ofthe mother. Methods-The cases were children with spina bifida aperta born between 1980 and 1992 from nine hospitals in the Netherlands. The controls were children born healthy in the same period as the cases, from hospitals and from the general population. Data collection was...

Abstract Objective Although most cases with spina bifida cystica could be closed by primary skin closure or without undermining its edges, about 25% of patients have large defects not amenable for these simple methods. We conducted this study to review our techniques in closing defects. Methods retrospectively reviewed the data consecutive 21 diagnosed setting. According surface area defect, ap...