Results 111 to 120 of about 111,118 (342)
Congenital short bowel syndrome: Clinical aspects by systematic review
JPGN Reports, EarlyView.Abstract Objectives Congenital short bowel syndrome (CSBS) is a rare intestinal disorder characterized by inborn shortening of the bowel with mainly mutations in Coxsackie and Adenovirus receptor‐like membrane protein (CLMP) and Filamin A (FLNA) genes.
Barblin Remund +2 more
wiley +1 more source
Clinical Case ReportsKey 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
Combined Duodenal Atresia and Pure Esophageal Atresia
, 2015 Combined duodenal atresia and pure esophageal atresia is a rare combination which has been reported only 13 times previously in the literature. Although this pair of congenital anomalies is amenable to current treatment strategies, it is often associated
Alaish SM
core +1 more source
Genetic sequencing of children with malrotation and midgut volvulus: A cross‐sectional study
JPGN 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
JEADV 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
Российский журнал гастроэнтерологии, гепатологии, колопроктологии, 2012 Aim of investigation. Analysis of phenotypical and genotypical signs in neonates with atresia of duodenum and other parts of the small intestine.Material and methods.
O. K. Botvin'yev, A. V. Eremeeva
doaj
, 2009 Abstrak. Atresia koana adalah oldusi membran atau tulang kongenital dari satu atau kedua koana akibat gagalnya membran bukonasalis untuk membelah sejak embrionaJ.2A Manifestasi klinis atresia koana bisa anterior.posterior, unilateral,bilateral ...
Teuku Husni T.R
core
The Kaohsiung Journal of Medical Sciences, EarlyView.ABSTRACT This retrospective study aimed to explore the value of DAT‐FAT serological profiles confirmed by AET in classifying neonatal jaundice, evaluating its severity, and guiding clinical management. A total of 915 jaundiced newborns (584 pathological, 331 physiological) admitted from July 2018 to August 2021 were included.
Tian‐Ge Wu +7 more
wiley +1 more source