Schmitt H P, Kawakami M
Brain Dev. 1982;4(6):469-74. doi: 10.1016/s0387-7604(82)80075-2.
Report of a newborn infant with a caudal regression syndrome and a large myelocystocele. A small part of the transitional zone between the normal spinal cord and the myelocystocele displayed a triploid cord in cross sections, suggesting a kind of "triastematomyelia," which was, however, finally considered rather to represent a special form of diastematomyelia than a true threefold split of the spinal cord. The probable pathogenetic background of the condition is discussed.
一名患有尾椎退化综合征和巨大脊髓脊膜膨出的新生儿报告。在正常脊髓与脊髓脊膜膨出之间的过渡区的一小部分，横切面上显示为三倍体脊髓，提示一种“三脊髓纵裂”，然而，最终认为这更像是脊髓纵裂的一种特殊形式，而非真正的脊髓三重分裂。文中讨论了该病症可能的发病机制背景。
