Results 101 to 110 of about 132,899 (238)

Congenital Intraoral Synechiae: A Scoping Review of Airway, Feeding, and Surgical Management

open access: yesOtolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective To map the existing literature on congenital intraoral synechiae and summarize reported anatomic patterns, clinical presentation, associated anomalies/syndromes, and outcomes to inform standardized diagnostic and therapeutic approaches. Data Sources PubMed, CINAHL, Embase, Web of Science, and Google Scholar were searched from January
Jason Bernier, Mathieu Bergeron
wiley   +1 more source

Prenatal Exome Sequencing Identifies Dual Maternal‐Fetal Diagnosis of HbF Mission Bay, a Novel HBG2 Variant Associated With Methemoglobinemia, Hypoxia and Hemolytic Anemia

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Prenatal exome sequencing (ES) can establish rare genetic diagnoses in a fetus but may also lead to occult genetic diagnosis in a biological parent. We present a case of dual fetal and maternal diagnosis by prenatal ES, in a fetus with unexplained anemia and in a pregnant patient with sickle cell disease (SCD) and recurrent unexplained hypoxia.
Matthew A. Shear   +6 more
wiley   +1 more source

Retroflexão e evisceração da vesícula urinária decorrente de ruptura dos órgãos genitais em cadela Retroflexion and evisceration of the urinary bladder due to rupture of the genitals organs in bitch

open access: yesCiência Rural, 2013
O presente relato descreve o caso de uma fêmea canina, adulta, sem raça definida, que havia parido há 45 dias e, posteriormente, apresentou ruptura uterina e vaginal com retroflexão e evisceração de bexiga, condição raramente observada em cadelas.
Bruna Pinto Coutinho   +6 more
doaj  

Leiomioma retroperitoneal

open access: yesRevista Colombiana de Cirugía
Los leiomiomas uterinos son la neoplasia uterina más frecuente en la mujer y se desarrollan a partir de células musculares lisas; rara vez se localizan en el retroperitoneo 1.
Franco Rafael Ruiz-Echeverría   +1 more
doaj   +1 more source

Hemophilia A: An Ideal Disease for Prenatal Therapy

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Hemophilia A (HA) is the most common inherited coagulation defect. Current state‐of‐the‐art treatment consists of frequent administration of prophylactic infusions of coagulation factor VIII (FVIII) protein or bispecific antibodies that replace the cofactor function of FVIIIa to maintain hemostasis. However, these treatments are far from ideal,
Christopher D. Porada   +2 more
wiley   +1 more source

UNIONES EN HENDIDURA Y SU PAPEL FUNCIONAL EN EL TRACTO REPRODUCTOR FEMENINO

open access: yesRevista Chilena de Obstetricia y Ginecología, 2004
En el aparato reproductor femenino se expresan diferentes conexinas (Cxs), proteínas que forman canales de uniones en hendidura (CUH) entre células en contacto, permitiendo la coordinación de respuestas metabólicas y/o eléctricas de grupos celulares. Los
María C. Brañes O   +3 more
doaj  

Efectos del útero bicorne en la fertilidad [PDF]

open access: yes
El útero bicorne es una anomalía congénita del tracto reproductivo femenino que puede impactar significativamente la fertilidad. Esta malformación uterina, caracterizada por un útero con dos cavidades separadas, puede presentar diversas formas de ...
Sebastián Leonardo Valle Chimbo   +3 more
core  

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell   +6 more
wiley   +1 more source

Cirugía conservadora del útero

open access: yesCirugía del Uruguay, 1973
En el trabajo se repasan las indicaciones y las técnicas destinadas a: 1) Mantener las funciones del órgano durante las intervenciones que se realizan sobre él; 2) Tratar las afecciones que alteran dichas funciones.
Serafín V Pose
doaj  

Attitudes Toward Prenatal Interventions in the Fanconi Anemia Community

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective In‐utero cell and gene therapies may offer prenatal treatment options for inherited diseases. Preclinical data suggests in‐utero (IU) hematopoietic stem cell transplantation (HSCT) could prevent Fanconi anemia (FA) related bone marrow failure without genotoxic conditioning or immune suppression.
Tony Lum   +4 more
wiley   +1 more source

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