ライフサイエンスコーパス: myelomeningocele

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1 ent questions that surround the newborn with myelomeningocele.

2 n which the affected child had a lumbosacral myelomeningocele.

3 ic patients with non-syndromic lumbar-sacral myelomeningocele.

4 assignment of a lesion level in a fetus with myelomeningocele.

5 nts who have undergone fetal repair of their myelomeningoceles.

6 Seven patients with myelomeningocele, aged 4-19 years, with high-pressure or

7 ccurs in a large percentage of children with myelomeningocele and is the leading cause of death in th

8 congenital central hypoventilation syndrome, myelomeningocele, and Prader-Willi syndrome.

9 In this series of patients, fetal myelomeningocele closure resulted in improvement in hind

10 Infants with myelomeningocele continue to be a management dilemma for

11 r study suggests that intrauterine repair of myelomeningocele decreases the incidence of hindbrain he

12 defect; however, whether in utero repair of myelomeningocele improves neurologic outcome in infants

13 Myelomeningocele (MMC) is a devastating spinal cord birt

14 or congenital anomalies, including repair of myelomeningocele (MMC, n=51), resection of intrathoracic

15 The effect of early fetal closure of myelomeningocele on hindbrain herniation is unknown.

16 Prenatal surgery for myelomeningocele reduced the need for shunting and impro

17 ple of 29 study patients with isolated fetal myelomeningocele referred for intrauterine repair that w

18 first 100 fetuses who underwent intrauterine myelomeningocele repair were the basis for this study.

19 Prenatal repair of myelomeningocele, the most common form of spina bifida,

20 Spina bifida (SB) patients afflicted with myelomeningocele typically possess a neurogenic urinary

21 nts who have undergone fetal repair of their myelomeningocele with respect to neurodevelopmental outc

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