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1 assignment of a lesion level in a fetus with myelomeningocele.
2 ent questions that surround the newborn with myelomeningocele.
3 n which the affected child had a lumbosacral myelomeningocele.
4 ic patients with non-syndromic lumbar-sacral myelomeningocele.
5 nts who have undergone fetal repair of their myelomeningoceles.
6 and White (136 participants [68.0%]) and had myelomeningocele (125 participants [62.5%]).
7 tions in the ARMC5 gene in 511 patients with myelomeningocele, a severe form of spina bifida.
8                     Of the 161 children with myelomeningocele aged 5 to 10 years old enrolled in MOMS
9                          Seven patients with myelomeningocele, aged 4-19 years, with high-pressure or
10 ccurs in a large percentage of children with myelomeningocele and is the leading cause of death in th
11 s or older with a diagnosis of spina bifida (myelomeningocele and nonmyelomeningocele) whose primary
12 congenital central hypoventilation syndrome, myelomeningocele, and Prader-Willi syndrome.
13            In this series of patients, fetal myelomeningocele closure resulted in improvement in hind
14                                 Infants with myelomeningocele continue to be a management dilemma for
15 r study suggests that intrauterine repair of myelomeningocele decreases the incidence of hindbrain he
16 s indicate the benefit of prenatal repair of myelomeningocele for school-aged children.
17 of prenatal vs standard postnatal repair for myelomeningocele, found that prenatal repair reduced hyd
18  defect; however, whether in utero repair of myelomeningocele improves neurologic outcome in infants
19 on groups may elevate the risk of developing myelomeningocele in the study cohort.
20                                              Myelomeningocele (MMC) affects one in 1000 newborns annu
21                         Open spina bifida or myelomeningocele (MMC) is a devastating neurologic conge
22                                              Myelomeningocele (MMC) is a devastating spinal cord birt
23        To investigate the association of the myelomeningocele (MMC) volume with prenatal and postnata
24 or congenital anomalies, including repair of myelomeningocele (MMC, n=51), resection of intrathoracic
25         The effect of early fetal closure of myelomeningocele on hindbrain herniation is unknown.
26 ries); the defects included two instances of myelomeningocele, one of anencephaly, one of encephaloce
27                         Prenatal surgery for myelomeningocele reduced the need for shunting and impro
28 ple of 29 study patients with isolated fetal myelomeningocele referred for intrauterine repair that w
29 first 100 fetuses who underwent intrauterine myelomeningocele repair were the basis for this study.
30  functioning benefits of prenatal repair for myelomeningocele reported at age 30 months persisted int
31                            The Management of Myelomeningocele Study (MOMS), a randomized clinical tri
32                            The Management of Myelomeningocele Study Follow-up (MOMS2) was conducted i
33                           Prenatal repair of myelomeningocele, the most common form of spina bifida,
34    Spina bifida (SB) patients afflicted with myelomeningocele typically possess a neurogenic urinary
35 nts who have undergone fetal repair of their myelomeningocele with respect to neurodevelopmental outc