Results 31 to 40 of about 726,961 (271)

A Case of Secondary FSGS due to Chronic Chloride Diarrhea [PDF]

Childhood Kidney Diseases, 2016
Congenital chloride diarrhea (CLD) is a rare autosomal recessive disease that is difficult to diagnose. CLD requires early treatment to correct electrolyte imbalance and alkalosis and to prevent severe dehydration. Renal injury is clearly associated with
Byung Kwan Kim, Hyun Soon Lee, Hyung Eun Yim, Hae Il Cheong, Kee Hwan Yoo   +4 more
doaj   +1 more source

Surgical treatment of renovascular hypertension [PDF]

Zagazig University Medical Journal, 2020
Background: Renovascular hypertension is the commonest form of secondary hypertension. It occurs in less than 5 % of all hypertensive population. There are two forms of renovascular hypertension: Atherosclerotic and fibromuscular dysplasia.
Tarek Salem, Mohamed Salem, Amr Salem, Sameh Moustafa   +3 more
doaj   +1 more source

HYPOPARATHYROIDISM, DEAFNESS, AND RENAL DYSPLASIA

, 2014
Background. HDR syndrome is an autosomal dominant disorder characterized by hypoparathyroidism, sensorineural deafness, and renal dysplasia caused by mutation of the GATA3 ...
COSKUN, H., ERSOZ, H. O., EREM, CİHANGİR, CIVAN, NADİM, Nuhoglu, I., KOCAK, MUSTAFA   +5 more
core   +1 more source

TP63‐mutation as a cause of prenatal lethal multicystic dysplastic kidneys

Molecular Genetics & Genomic Medicine, 2020
Background Ectrodactyly‐ectodermal dysplasia‐clefting syndrome 3 (EEC) is one of the six overlapping syndromes caused by mutations in the tumor protein p63 gene (TP63). EEC is suspected when patients have cleft hands or feet, polydactyly, and syndactyly,
Isabel Friedmann, Carla Campagnolo, Nancy Chan, Ghislain Hardy, Maha Saleh   +4 more
doaj   +1 more source

Large Multicystic Dysplastic Kidney Mimicking a Large Cystic Renal Neoplasm [PDF]

Journal of Clinical and Diagnostic Research, 2017
Multicystic Dysplastic Kidney (MCDK) is one of the most common renal conditions seen in paediatric population. The natural history typically involves involution and many of the patients with unilateral disease may actually never become symptomatic.
Priyank Yadav, Sanjoy Kumar Sureka, M S Ansari, Rahul Soni, Hira Lal   +4 more
doaj   +1 more source

MAGI3 Acts as an Intestinal Epithelial Gatekeeper in Inflammation‐Associated Colorectal Cancer by Suppressing the STAT3‐CCL2 Axis and TAM‐Mediated Immunosuppression

Advanced Science, EarlyView.
Our study identifies MAGI3 as an intestinal epithelial gatekeeper that restrains inflammation‐associated colorectal tumorigenesis but is itself suppressed under highly inflammatory conditions. MAGI3 deficiency activates the STAT3‐CCL2 signaling, thereby promoting TAM‐mediated immunosuppression and inflammation‐associated colorectal tumor progression ...
Yumeng Yang, Zhigang Bai, Haibo Wang, Yu Guo, Yan Zhang, Meihan Hu, Shuaikang Fan, Ran Song, Tongmei Zhang, Mengqi Deng, Xiaomei Yang, Zhongtao Zhang, Junqi He   +12 more
wiley   +1 more source

Bilateral renal artery stenosis treated with drug-eluting balloon angioplasty in unique treatment

Radiology Case Reports, 2019
Renal artery stenosis commonly manifests with hypertension refractory to medical treatment. We report a case of renal artery stenosis occurring in a 19-year-old female patient who presented with extremely high blood pressure and bilateral renal stenosis ...
Daniele Morosetti, MD, Marcello Chiocchi, MD, PhD, Federica De Crescenzo, MD, Adolfo D'Onofrio, MD, Arezia Di Martino, MD, Armando Raso, MD, Roberto Floris, MD, PhD, Roberto Gandini, MD, PhD   +7 more
doaj   +1 more source

Systematic Cardiac Phenotyping of Patients With Copy Number Variants in the 15q11.2 Breakpoint 1 to Breakpoint 2 Region: A Retrospective Cohort Study From Nine Pediatric Cardiac Centers

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Microdeletions impacting 15q11.2 breakpoint (BP) 1 to BP2, adjacent to the Prader–Willi critical region, have previously described neuropsychiatric associations, with potential low penetrance presentations of congenital heart disease (CHD) also identified.
Morgan B. Wright, Maria B. Padua, Lindsey R. Helvaty, Kim L. McBride, Gabrielle Geddes, Vidu Garg, Seema R. Lalani, Stephanie Burns Wechsler, Jennelle C. Hodge, Benjamin J. Landis, Stephanie M. Ware   +10 more
wiley   +1 more source

HEMOSTATIC SYSTEM DISORDERS IN CHILDREN WITH HYDRONEPHROSIS AND WAYS OF DRUG THERAPY

Педиатрическая фармакология, 2011
In hydronephrosis, dysplasia of connective tissue results in hemostatic system disorders manifesting themselves as hemorrhagic mesenchimal dysplasia. The article analyses the coagulograms of 63 children with renal hydronephrosis in pre-school age.
V.A. Dudarev, E.V. Portnyagina, A.G. Timofeeva, I.V. Kirgizov   +3 more
doaj   +2 more sources

PAX2 Expression in Renal Dysplasia [PDF]

, 2007
Background : Renal dysplasia is the abnormal development of the kidney. The condition is usually detected in childhood along with other urinary tract anomalies, but can remain unnoticed until adulthood.
정현주, 정우희, 홍순원
core