Results 101 to 110 of about 2,629 (212)

Long-Term Outcomes of Trabeculectomy Augmented with Mitomycin C Undertaken within the First 2 Years of Life [PDF]

, 2015
To evaluate the long-term effectiveness and safety of mitomycin C (MMC)–augmented trabeculectomy undertaken within the first 2 years of life for the surgical management of glaucoma.
Bunce, C, Chiang, M, Jayaram, H, Khaw, PT, Papadopoulos, M, Pooley, F, Scawn, R, Strouthidis, NG   +7 more
core   +1 more source

The Role of Soluble Urokinase Plasminogen Activator Receptor (suPAR) as an Early Indicator of Mortality in Pediatric Septic Shock

Journal of Clinical Laboratory Analysis, Volume 38, Issue 9, May 2024.
Despite advancements in antibiotic therapy and resuscitation protocols, sepsis and septic shock remain major contributors to morbidity and mortality in children. Employing plasma suPAR levels to discriminate between mortality and survival, a threshold of ≥7.0 ng/mL demonstrated a sensitivity of 90.9% and specificity of 71.0%. In pediatric septic shock,
Caner Turan, Ali Yurtseven, Pinar Yazici Ozkaya, Elif Azarsiz, Eylem Ulas Saz   +4 more
wiley   +1 more source

Adams–Oliver syndrome: About a case

Clinical Case Reports, Volume 12, Issue 4, April 2024.
Key Clinical Message We report the case of a newborn with aplasia cutis congenita characterized by the absence of skin in the left parietal region, superficial dilatation of the scalp veins, facial dysmorphia, limb anomalies, and severe intrauterine growth retardation.
John Mambo Itongwa, Moise Mbaluku Colombe, Helene Bukuru, Niyongeko Deogratias, Cédric Irenge Matabaro, Fernand Manga Opondjo, Viviane Feza Bianga, Ndayishimye Alice   +7 more
wiley   +1 more source

Cutis marmorata telangiectatica congenita in a preterm newborn - Case report and literature review. [PDF]

Iran Red Crescent Med J, 2012
Matic A, Pricic S, Matic M, Velisavljev Filipovic G, Ristivojevic A.   +4 more
europepmc   +2 more sources

Concurrent Sturge-Weber syndrome, facial infantile hemangioma, and cutis marmorata telangiectatica congenita. [PDF]

, 2017
We present a unique case of 3 vascular malformations-Sturge-Weber syndrome (SWS), facial infantile hemangioma (IH), and cutis marmorata telangiectatica congenita (CMTC)-with dermatologic manifestations presenting in the same patient. This case highlights
Poliak, Nina, Rainey, Anthony
core   +1 more source

Cutis marmorata telangiectasica congenita: Presentación de un caso y Revisión de la literatura

Revista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica, 1996
Presentamos el caso de una recién nacida con cutis marmorata telangiectásica congénita, rara anormalidad cutánea benigna de etiología desconocida y que se caracteriza por un patrón reticular rojo a púrpura al nacer que frecuentemente mejora con la edad,
Ricardo Rojas López, Alvaro Acosta de Hart   +1 more
doaj  

Van Lohuizen Syndrome – A Case Report with a Diagnostic Delay of Four Years [PDF]

, 2018
BACKGROUND: Cutis marmorata telangiectatic congenital or Van Lohuizen syndrome is a rare vascular disorder that may be associated with other congenital malformations.
França, Katlein, Lotti, Torello, Tchernev, Georgi, Wollina, Uwe   +3 more
core   +3 more sources

Current concepts of polymicrogyria [PDF]

, 2010
Polymicrogyria is one of the most common malformations of cortical development. It has been known for many years and its clinical and MRI manifestations are well described.
A Jansen, A. James Barkovich, AJ Barkovich, AJ Barkovich, AJ Barkovich, AJ Barkovich, AJ Barkovich, AJ Barkovich, AJ Barkovich, AJ Barkovich, AJ Barkovich, AL Gropman, AS Brooks, B Chang, BS Chang, C Englund, C Moore, C Raybaud, DE Michele, EPM Oliveira, F Giuliano, G Mirzaa, G Wieck, I Pascual-Castroviejo, I Pascual-Castroviejo, IA Aligianis, J Aicardi, J Aicardi, J Hallervorden, J Takanashi, JM Graham Jr, KW Gripp, L Baala, L Garavelli, L Villard, M Nassogne, M Warburg, MG Norman, MM Guerreiro, N Hayashi, N Robin, P Evrard, P Roll, PM Bingham, PS Becker, R Borgatti, R Guerrini, R Guerrini, R Guerrini, R Guerrini, R Guerrini, R Kuzniecky, R Kuzniecky, R Wright, RH Caraballo, RJ Leventer, S Ferdinandusse, S Li, SA Moore, U Moog, WB Dobyns, X Piao, XH Jaglin, Y Rolland   +63 more
core   +4 more sources

A oxigenoterapia hiperbárica nas lesões neuro-músculoesqueléticas: um estudo retrospetivo [PDF]

, 2018
Projeto de Graduação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Licenciada em FisioterapiaObjetivo: Efetuar um levantamento de dados, através de uma análise retrospetiva, sobre a eficácia da ...
Silva, Catarina Sousa da
core  

Phakomatosis pigmentovascularis: A clinical profile of 11 Indian patients

Indian Journal of Dermatology, 2019
Introduction: Phakomatosis pigmentovascularis (PPV) is a rare congenital syndrome characterized by the simultaneous presence of capillary malformation and pigmentary nevi.
Abhijit Dutta, Sudip Kumar Ghosh, Debabrata Bandyopadhyay, Dibyendu Bikash Bhanja, Surajit Kumar Biswas   +4 more
doaj   +1 more source