Results 21 to 30 of about 534,986 (305)

Changing Mortality in Congenital Heart Disease

Journal of the American College of Cardiology, 2010
This study sought to characterize temporal trends in all-cause mortality in patients with congenital heart disease (CHD).Historically, most deaths in patients with CHD occurred in early childhood. Notable advances have since been achieved that may impact on mortality trends.We conducted a population-based cohort study of patients with CHD in Quebec ...
Khairy, Paul, Ionescu-Ittu, Raluca, Mackie, Andrew S., Abrahamowicz, Michal, Pilote, Louise, Marelli, Ariane J.   +5 more
openaire   +2 more sources

Nonimmune Hydrops Fetalis and Early Skeletal Changes in Congenital Syphilis: Case Series and Review of Literature [PDF]

Pediatric Infectious Disease
Aim and background: Syphilis remains the most common congenital infection in the world. During pregnancy, syphilis is associated with numerous findings, including placentomegaly, hepatomegaly, polyhydramnios, fetal nonimmune hemolytic anemia, and hydrops
Kruti N Shah, Shwetal Bhatt, Vaishali Chanpura   +2 more
doaj   +1 more source

Alteration of cystic airway mesenchyme in congenital pulmonary airway malformation. [PDF]

, 2019
Congenital pulmonary airway malformation (CPAM) is the most common congenital lesion detected in the neonatal lung, which may lead to respiratory distress, infection, and pneumothorax.
Jiang, Yi, Lou, Jianlin, Luo, Yongfeng, Moats, Rex, Pryhuber, Gloria S, Shi, Wei, Tang, Yang, Wang, Larry L, Warburton, David, Zhou, Shengmei   +9 more
core   +3 more sources

Bathing trunk naevus: a case report with dermoscopic findings in a brown child

Pigment International, 2021
Giant congenital melanocytic naevus is a naevus measuring more than 20 cm in adulthood. Its incidence is 1:20,000 and is more common in girls. Bathing trunk naevus, a specific form of giant congenital melanocytic naevus is even rarer with incidence of 1 ...
Megha Shankar, Sambasiviah Chidambara Murthy   +1 more
doaj   +1 more source

MEF2C regulates outflow tract alignment and transcriptional control of Tdgf1 [PDF]

, 2016
Congenital heart defects are the most common birth defects in humans, and those that affect the proper alignment of the outflow tracts and septation of the ventricles are a highly significant cause of morbidity and mortality in infants.
Barnes, Ralston M., Black, Brian L., Harris, Ian S., Jaehnig, E., McCulley, David J., Norris, Russell A., Rojas González, Anabel, Sauls, Kimberly, Schachterle, William, Sinha, Tanvi   +9 more
core   +1 more source

Prenatal detection of congenital high airway obstruction syndrome with encephalocele

Indian Journal of Radiology and Imaging, 2016
Congenital high airway obstruction syndrome (CHAOS) causes secondary morphological changes which can be detected on ultrasound. Here we report a case of congenital high airway obstruction with an occipital encephalocele detected at 23 weeks of gestation.
Laxmi Devi Padmanabhan, Sheela Nampoothiri   +1 more
doaj   +1 more source

Imaging of congenital lung diseases presenting in the adulthood: a pictorial review

Insights into Imaging, 2021
Congenital lung diseases in adults are rare diseases that can present with symptoms or be detected incidentally. Familiarity with the imaging features of different types of congenital lung diseases helps both in correct diagnosis and management of these ...
Gamze Durhan, Selin Ardali Duzgun, Meltem Gülsün Akpınar, Figen Demirkazık, Orhan Macit Arıyürek   +4 more
doaj   +1 more source

An anatomical classification of congenital proximal radioulnar synostosis based on retrospective MRI measurement combined with radiography

Scientific Reports, 2022
Existed classifications of congenital proximal radioulnar synostosis (PRUS) mainly focus on osseous changes and do not cover all types of congenital PRUS, ignoring the role and developing status of the supinator.
Jin Li, Kailei Chen, Jing Wang, Yueming Guo, Saroj Rai, Xin Tang, Chinese Multi-center Pediatric Orthopedic Study Group (CMPOS)   +6 more
doaj   +1 more source

Altered Spontaneous Brain Activity and Network Property in Patients With Congenital Monocular Blindness

Frontiers in Neurology, 2022
Individuals with congenital monocular blindness may have specific brain changes since the brain is prenatally deprived of half the normal visual input.
Jingwen Ding, Xiaoxia Qu, Jing Cui, Jie Dong, Jian Guo, Junfang Xian, Dongmei Li   +6 more
doaj   +1 more source

ARIX and PHOX2B polymorphisms in patients with congenital superior oblique muscle palsy. [PDF]

, 2005
To identify ARIX gene and PHOX2B gene polymorphisms in patients with congenital superior oblique muscle palsy, 3 exons of the ARIX gene and PHOX2B gene were sequenced by genomic DNA amplification with polymerase chain reaction (PCR) and direct sequencing
Fujiwara, hirotake, Hasebe, Satoshi, Jiang, Yan, Matsuo, Toshihiko, Ohtsuki, Hiroshi, Yasuda, Tatsuji   +5 more
core   +1 more source