Results 61 to 70 of about 6,051 (212)

Kyphectomy for congenital kyphosis due to meningomyelocele: a case treated with a modified approach to skin healing [PDF]

, 2012
This study is a case report of a meningomyelocele patient with congenital kyphosis who was treated with kyphectomy and a special approach to soft tissue healing.
Köse, Kamil Çağrı, İnanmaz, Mustafa Erkan   +1 more
core   +2 more sources

Bilateral propeller flap closure of large meningomyelocele defects

, 2014
PubMedID: 24918736Background: Meningomyelocele is a defect of the spinal cord, vertebral spine, and overlying skin and is the most common form of spinal dysraphism.
Uysal A.C., Borman H., Çöloglu O., Özkan B., Çöloglu H.   +4 more
core   +1 more source

Cutaneous markers of spinal dysraphism: A cross sectional study

Indian Journal of Paediatric Dermatology, 2018
Background: Spinal dysraphism is a rare condition where there are many cutaneous markers which will help a dermatologist to arrive at early diagnosis and prevent complications.
Farhana Tahseen Taj
doaj   +1 more source

Short‐ and Long‐Term Outcomes of Prenatally Identified Congenital Aqueductal Stenosis by Fetal MRI

Prenatal Diagnosis, Volume 44, Issue 13, Page 1574-1584, December 2024.
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, Usha D. Nagaraj, Beth M. Kline‐Fath, Karin S. Bierbrauer, Mounira Habli, Charu Venkatesan   +5 more
wiley   +1 more source

Long‐term survival of an infant with complete tetraploidy: A case report

American Journal of Medical Genetics Part A, Volume 194, Issue 11, November 2024.
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, Junko Yoshimoto, Daisaku Morimoto, Hirokazu Wanatabe, Yosuke Washio   +4 more
wiley   +1 more source

Success Rate and Predicting Factors for Repeated High‐Dose Intradetrusor Dysport Injections in Children With Neurogenic Bladder: A Retrospective Study

Neurourology and Urodynamics, Volume 43, Issue 8, Page 2140-2146, November 2024.
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, Roy Morag, Tal May, Dmitry Khunovitz, David Ben Meir   +4 more
wiley   +1 more source

The contribution of de novo coding mutations to meningomyelocele.

Meningomyelocele (also known as spina bifida) is considered to be a genetically complex disease resulting from a failure of the neural tube to close. Individuals with meningomyelocele display neuromotor disability and frequent hydrocephalus, requiring ...
Ashley-Koch, Allison, Tolias, Kimberley, Murray, Stephen, Major, Michael B, Kingsmore, Stephen, Jiang, Nan, Meave, Naomi, Noureldeen, Mahmoud M, Gee, Heon Yung, Zaki, Maha, Kara, Bülent, Shuldiner, Alan, Patel, Arzoo, Finnell, Richard H, Vong, Keng Ioi, Stevenson, Roger, Blanco, Francisco A, Capra, Valeria, Schroeder, Sarah, Plutzer, Isaac, Ashley-Koch, Allison E, Salem, Aida, Le, Joan, Murray, Stephen A, Meltzer, Hal S, Mumtaz, Sara, Banka, Niyati, Mutchinick, Osvaldo M, Ahmed, Awais, Issa, Mahmoud Y, Northrup, Hope, Major, Michael, Melikishvili, Gia, Bot, Gyang Markus, Bagga, Krisha, Xu, Libin, Machado, Helio R, Blanco, Francisco, Shril, Shirlee, Gleeson, Joseph, Kingsmore, Stephen F, Machado, Helio, Jhamb, Ishani, Rhee, Soeun, Kirmani, Salman, Shuldiner, Alan R, Salem, Aida M S, Lupo, Philip, Wallingford, John, Ha, Yoo-Jin Jiny, Friedman, Liana, Issa, Mahmoud, Hanak, Brian, Noureldeen, Mahmoud, Tolias, Kimberley F, Magana, Tony, Araujo, Camila, Stevenson, Roger E, Medina-Bereciartu, José Ramón, Wallingford, John B, Meltzer, Hal, Gleeson, Joseph G, Barrows, Chelsea, Koch, Allison, Kolvenbach, Caroline, Au, Kit Sing, Khara, Mulazim Hussain, Salimi-Dafsari, Hormos, Spina Bifida Sequencing Consortium, Tkemaladze, Tinatin, Phillips, H. Westley, Tang, Isaac, Kibar, Zoha, Lee, Sangmoon, Kim, Sangwoo, Zaki, Maha S, Gonda, David, Finnell, Richard, Jiwani, Fiza, Marwan, Ahmed I, Hildebrandt, Friedhelm, Güneş, Ayfer Sakarya, Jeong, Hui Su, Miller, W. Todd, Le, Joan T, Lee, Ji Eun, Miller, W Todd, Howarth, Robyn, Strain, Madison, Yurrita, Anna, Nisal, Ashna, Benoit, Béatrice, Alkelai, Anna, Marwan, Ahmed, Lee, Chanjae, Yu, Seyoung, Heffner, Caleb, Mutchinick, Osvaldo, Poüs, Christian, Wallace, Cassidy, Shin, Donghyuk, Takahashi, Yukitoshi   +101 more
core   +1 more source

Two cases of Jarcho-Levin syndrome with meningomyelocele and hydrocephalus

, 2017
WOS: 000406284600025Jarcho-Levin syndrome is associated with vertebra, central nervous system, cardiac, urinary and gastrointestinal system abnormalities.
Hacer Yapıcıoğlu, Yildirim, Pelin, Ece, Umit, Gülseren Bilen Yurdakul, Yurdakul, Gulseren Bilen, İkram Kavuncu, Kavuncu, Ikram, Celiloglu, Ozgu, Yapicioglu, Hacer, Özgü Celiloğlu, Ümit Ece, Pelin Yıldırım   +11 more
core   +1 more source

Local Flaps with Negative Pressure Wound Therapy in Secondary Reconstruction of Myelomeningocele Wound Necrosis

Plastic and Reconstructive Surgery, Global Open, 2018
Summary:. Major wound necrosis is an uncommon yet critical complication of meningomyelocele surgical repair with few reports available. Management is demanding and often requires further reconstructive surgery. We report a case of a neonate who developed
Chihena H. Banda, MD, Mitsunaga Narushima, MD, PhD, Ryohei Ishiura, MD, Minami Fujita, MD, Megumi Furuya, MD   +4 more
doaj   +1 more source

Sleep‐disordered breathing on respiratory polygraphy in neonates with spina bifida

Pediatric Pulmonology, Volume 59, Issue 11, Page 2829-2838, November 2024.
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, Christian Bieli, Patrice Grehten, Theres Moehrlen, Ueli Moehrlen, Vera Bernet, Cornelia Hagmann, Spina Bifida Study Group Zurich, Beate Grass   +8 more
wiley   +1 more source