Results 1 to 10 of about 101,613 (269)

Factors of immunodeficiency in children with trisomy 21 (Down syndrome): a modern paradigm of immune and non-immune mechanisms

Zdorovʹe Rebenka, 2018
Down syndrome is the most common genetic disorder. Children with trisomy 21 often suffer from severe, prolonged respiratory infections, which is an immune system defect.
O.L. Logvinova
doaj   +1 more source

A new type of lordosis and vertebral body compression in Gilthead seabream, Sparus aurata Linnaeus, 1758: aetiology, anatomy and consequences for survival [PDF]

, 2013
A new type of vertebral malformation is described, consisting of deformed cartilaginous neural and haemal processes and the compression and fusion of vertebral bodies. The malformation is designated as haemal vertebral compression and fusion (haemal VCF).
Georgiou, AN, Koumoundouros, G, Loizides, M, Somarakis, S, Witten, Paul   +4 more
core   +2 more sources

Gut dysmotility in functional gastrointestinal disorders. Potential for therapeutic adjustment in terms of clinical case management

Медицинский совет, 2020
Gastrointestinal motility disorders can be a leading pathogenetic factor contributing to the development of many common gastroenterological diseases. Motor disorders can be a pathogenetic mechanism of development of both organic pathology (developmental ...
I. G. Pakhomova
doaj   +1 more source

Prevalence of disorders recorded in Cavalier King Charles Spaniels attending primary-care veterinary practices in England [PDF]

, 2015
Concerns have been raised over breed-related health issues in purebred dogs, but reliable prevalence estimates for disorders within specific breeds are sparse.
Brodbelt, D C, Church, D B, McGreevy, P D, O'Neill, D G, Summers, J F, Thomson, P C   +5 more
core   +3 more sources

Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report

Italian Journal of Pediatrics, 2022
Background Contiguous gene deletion syndrome at Xp22.3 resulting in nullisomy in males or Turner syndrome patients typically encompasses the steroid sulfatase gene (STS) and contiguously located other genes expanding the phenotype.
Ingrid Anne Mandy Schierz, Mario Giuffrè, Marcello Cimador, Maria Michela D’Alessandro, Gregorio Serra, Federico Favata, Vincenzo Antona, Ettore Piro, Giovanni Corsello   +8 more
doaj   +1 more source

Congenital malformations at a referral hospital in Gorgan, Islamic Republic of Iran [PDF]

, 2005
This study recorded the rate of congenital malformations in 10 000 births at a referral hospital in Gorgan, Islamic Republic of Iran in 1998-99. The overall incidence of congenital malformations was 1.01% (1.19% in males and 0.76% in females).
Ahmadpour-Kacho, M., Golalipour, M.J., Vakili, M.A.   +2 more
core  

Evaluation of Incidence and Main Risk Factors of Major Congenital Anomalies in Hospitals Affiliated with Isfahan University of Medical Sciences during 1395

مجله اپیدمیولوژی ایران, 2020
Background and Objectives: Congenital anomalies are also known as birth defects and congenital disorders. Congenital anomalies occur in about 3-7% of the newborn babies worldwide.
M Saberi, M Hosseinpour, A Khaleghnejad Tabari, H Soori, MR Maracy   +4 more
doaj  

Novel cruzain inhibitors for the treatment of Chagas' disease. [PDF]

, 2012
The protozoan parasite Trypanosoma cruzi, the etiological agent of Chagas' disease, affects millions of individuals and continues to be an important global health concern.
Arkin, Michelle R, Doak, Allison, Durrant, Jacob D, Keränen, Henrik, McCammon, J Andrew, Ratnam, Joseline, Rogers, Kathleen E   +6 more
core   +1 more source

Congenital absence of the gallbladder in a child: a case report

Frontiers in Pediatrics
BackgroundCongenital absence of the gallbladder (CAGB) is an exceedingly rare embryological anomaly of the biliary system, with a complex etiology involving the failure of gallbladder formation during embryogenesis.
Xiao Wei, Liying You, Chun Liu, Xu Xu
doaj   +1 more source

Risks of hospitalization and drug consumption in children and young adults with diagnosed celiac disease and the role of maternal education: A population-based matched birth cohort study [PDF]

, 2016
Background: Celiac disease (CD) may affect healthcare use in children and young adults. Socio-economic factors may act as a confounder or effect modifier.
Canova, Cristina, Ludvigsson, Jonas F, Pitter, Gisella, Romor, Pierantonio, Simonato, Lorenzo, Zanier, Loris, Zanotti, Renzo   +6 more
core   +6 more sources