We describe three cases (one male and two females) of faun tail nevi, which is one of the most important cutaneous marker of spinal dysraphism. One of the patients presented with acro-osteolysis leading to auto amputation of the toes of the left foot, which required operative intervention. This lays stress on the early recognition of lumbar paraspinal skin lesions and early treatment to avoid i...

Retrospective analysis of B-mode spinal sonography in 15 pediatric patients with spinal dysraphism and caudal anomalies documents a high degree of accuracy in identifying the presence, site, size, and configuration of meningoceles; and slightly less accuracy in identifying extension of neural tissue into the meningocele and presence of concurrent lipoma. B-mode sonography is capable of displayi...

Background: Split Spinal cord Malformation (SSCM) is a form of spinal dysraphism in which any or all of the spinal cord, cauda equina, and filum terminale are divided by a bony or fibrous spur. There are two described types of SSCM, namely Types I and II. In Type I SSCM, there are separate hemi-cords contained in two dural sacs, separated by a bony spur; in Type II SSCM, there is a single dural...

We reviewed 104 consecutive cases of closed dysraphism in patients seen at one institution between December 1984 and June 1987. All patients had myelographic studies, and 43 had associated CT examinations. Clinical and surgical findings (64 patients) were correlated with myelographic information. Twenty-three patients (22%) with clinical or plain film findings compatible with dysraphism had nor...

Delayed and nondelayed bilateral bipedicled fasciocutaneous flaps in large meningomyelocele defects: a preliminary results Congenital fusion defects of the neural tube and the related structures are classified as spinal dysraphism. Meningomyelocele is a defect which is the most common form of spinal dysraphism and occurs at an approximate rate of 1 in 800-1000 live births. In untreated meningom...