Results 71 to 80 of about 8,360 (205)
Short‐ and Long‐Term Outcomes of Prenatally Identified Congenital Aqueductal Stenosis by Fetal MRI
ABSTRACT Objective Providing accurate prenatal prognostication for expectant parents is challenging due to limited literature on factors impacting outcomes in children with congenital aqueductal stenosis (CAS). This study stratified CAS patients into isolated or complex categories (presence of additional intra‐ or extra‐cranial anomalies or genetic ...
Noah J. Smith +5 more
wiley +1 more source
Long‐term survival of an infant with complete tetraploidy: A case report
Abstract We present the case of a girl with complete tetraploidy who has survived to her present age of 4 years and 1 month. Infants with complete tetraploidy have been described to have a limited lifespan owing to complications. We report her characteristics, medical history, and development.
Tomoka Okamura +4 more
wiley +1 more source
ABSTRACT Objectives Evaluating the effectiveness and safety of repeated high‐dose intradetrusor abobotulinumtoxin A (Dysport®) injections for the treatment of pediatric neurogenic bladders refractory to medications. Design Retrospective interventional study.
Yossi Ventura +4 more
wiley +1 more source
Sleep‐disordered breathing on respiratory polygraphy in neonates with spina bifida
Abstract Introduction Studies have shown a high prevalence of sleep‐disordered breathing (SDB) in children with spina bifida. International standards for regular testing for SDB in this population are lacking. While there are studies investigating the prevalence of SDB in children with spina bifida, there are close to no studies in neonates.
Lorine Wachsmuth +8 more
wiley +1 more source
Sacral neuromodulation in children and adolescents with defecation disorders
In this prospective study of a pediatric population, sacral neuromodulation (SNM) shows efficacy in up to 90% of patients with refractory chronic constipation and fecal incontinence. Indications for SNM might therefore be expanded to patients with Hirschsprung's disease and congenital neuronal defecation disorders.
Manuel Besendörfer +6 more
wiley +1 more source
We analyzed 31 children with myelomeningocele born between July 1990 and July 2000. Follow-up median was 24 months (6-68months). Only 2 mothers had a known etiologic factor (diabetes mellitus). Twelve had the correct prenatal diagnosis. All children were
Maria M.M. Ulsenheimer +7 more
doaj +1 more source
ABSTRACT ObjectivesTo determine if the lower‐extremity neurological motor function level in fetuses with open spina bifida deteriorates within the 4‐week interval between a first prenatal motor assessment at around 22 weeks of gestation and a second evaluation, prior to ‘late’ prenatal surgery, defined as surgery at 26–28 weeks and, in certain ...
L. Trigo +6 more
wiley +1 more source
Therapeutic use of stem cells in congenital anomalies: A pilot study
Introduction: Stem cells with potential to transform into healthy cells and repair damaged cells may prove beneficial in various congenital malformations. Aim: To explore the use of stem cells in liver cirrhosis and meningomyelocele.
Sharma Shilpa +5 more
doaj
Primary germ cell tumours of the mediastinum: A review with emphasis on diagnostic challenges
Primary mediastinal germ cell tumours encompass five histological subtypes: seminoma, embryonal carcinoma, teratoma, yolk‐sac tumour and choriocarcinoma. Seminomas consist of medium‐sized cells with clear to eosinophilic cytoplasm and prominent nucleoli.
Alexander Fichtner +3 more
wiley +1 more source
Spina Bifida and Carbamazepine
The records of all pregnant Medicaid recipients in Michigan who were taking anti-epileptic agents during pregnancy were studied at the Center for Drug Evaluation and Research, Food and Drug Administration, Rockville, Maryland.
J Gordon Millichap
doaj +1 more source

