Diastematomyelia in two sisters.
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Diastematomyelia is a rare spinal cord anomaly that usually occurs in a non-syndromal, sporadic manner; however, few familial cases have been reported. We report on diastematomyelia in 2 sisters with variable expressivity. The spinal column is divided by osseous or fibrous tissue. This may be responsible for the variable expressivity. Most cases previously reported were females. This suggests X-linked dominant inheritance with lethality in hemizygous males or female sex limitation of a multifactorial trait.
[1] E. Weiner,et al. PRENATAL DIAGNOSIS OF DIASTEMATOMYELIA: CASE REPORTS AND REVIEW OF THE LITERATURE , 1997, Prenatal diagnosis.
[2] G. Breningstall,et al. Hydrosyringomyelia and diastematomyelia detected by MRI in myelomeningocele. , 1992, Pediatric neurology.
[3] R. Byrne,et al. Diastematomyelia: prenatal ultrasonic appearances. , 1989, Clinical radiology.
[4] Z. Kapsalakis. DIASTEMATOMYELIA IN TWO SISTERS. , 1964, Journal of neurosurgery.