Results 71 to 80 of about 402,747 (185)

Colonic atresia in a newborn. Case Report

open access: yesCase Reports, 2018
Introduction: Colonic atresia is the least common type of intestinal atresia; however, it must be suspected in patients with partial or complete intestinal obstruction, failure to pass meconium, vomit and abdominal distension.
Diego Armando Montenegro Pinzon   +2 more
doaj   +1 more source

Atresia do Esôfago: Análise de casos em seis anos. [PDF]

open access: yes, 2007
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Machado, Thais Kroeff
core  

Type 3B jejunoileal atresia management at a tertiary hospital in northern Tanzania: A report of three cases

open access: yesClinical Case Reports
Key Clinical Message Jejunalileal atresia is a cause of intestinal obstruction in the newborn, hence a surgical emergency. Prenatal diagnosis can be made by simple obstetric ultrasound and postnatal by plain abdominal x‐ray to plan a multidisciplinary ...
Evance Salvatory Rwomurushaka   +3 more
doaj   +1 more source

Mitchell-Riley Syndrome Report of Novel Mutation and Review of the Literature

open access: yesJournal of Biochemical and Clinical Genetics, 2018
Background: Mitchell-Riley Syndrome (OMIM # 615710) is a rare autosomal recessive disorder, characterized by a genetic mutation in the RFX6 gene. Clinically it is presented with triad of neonatal diabetes, gall bladder agenesis/hypoplasia and intestinal
Nourah Alruqaie, Majid Alfadhel
doaj   +1 more source

Genetic sequencing of children with malrotation and midgut volvulus: A cross‐sectional study

open access: yesJPGN Reports, EarlyView.
Abstract Objectives Intestinal malrotation with midgut volvulus can cause a particularly severe form of pediatric intestinal failure and is often a cause of ultra‐short bowel syndrome (SBS), with longer dependence on parenteral nutrition. While malrotation can be found in several genetic syndromes, most occurrences of this condition are not associated ...
Jonathan A. Salazar   +9 more
wiley   +1 more source

Validation of the Investigator's Global Assessment Scale for Epidermolysis Bullosa Simplex

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Background There is a lack validated outcome measures to assess wound severity in epidermolysis bullosa simplex (EBS). Objectives To assess the reliability and validity of the Investigator's Global Assessment (IGA) scale and a newly developed palms/soles subscale through in‐clinic scoring and review of patient‐submitted photographs.
Pirunthan Pathmarajah   +13 more
wiley   +1 more source

Management of jejunoileal atresias: an experience at eastern Nepal

open access: yesBMC Surgery, 2010
Background Intestinal atresia is a common cause of neonatal intestinal obstruction, and management of this disease in limited setup of a developing country is very difficult.
Poudel Prakash   +5 more
doaj   +1 more source

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

Type-3B intestinal atresia in dizygotic twins: a case report

open access: yesJournal of Pediatric Surgery Case Reports
Introduction: Jejunoileal atresia is a rare cause of neonatal intestinal obstruction. Apple peel atresia (type IIIb) represents less than 5% of jejunoileal atresia cases and is exceptionally uncommon in twins.
Maher Alzaiem   +4 more
doaj   +1 more source

Diagnostic Yield of Post‐Mortem Fetal Micro‐CT for Abdominal and Pelvic Anomalies

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective(s) This study aims to document the abdominal and pelvic anomalies that can be demonstrated using post mortem Micro‐CT, independent of whether the anomaly contributed to the main diagnosis or cause of death. Methods We retrospectively analyzed 1200 whole body post‐mortem fetal Micro‐CT scans in an unselected, consecutive cohort ...
Ian C. Simcock   +5 more
wiley   +1 more source

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