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Search Results for "Congenital Anomalies Associated With Uti"

02:54 EDT 22nd May 2013 | BioPortfolio

Original Source: Genetics of congenital anomalies of the kidney and urinary tract.

Congenital anomalies of the kidney and urinary tract (CAKUT) occur in 1 in 500 births and are a major cause of morbidity in children. Notably, CAKUT account for the most cases of pediatric end-stage renal disease and predispose the individual to hypertension and cardiovascular disease throughout life. Although some forms of CAKUT are a part of a syndrome or are associated with a positive family history, most cases of renal system anomalies are sporadic and isolated to the urinary tract. Broad phenotypic spe...

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Congenital Diseases

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Multiple Births Affected By Congenital Anomalies Have Doubled Since The 1980s

The number of congenital anomalies, or birth defects arising from multiple births has almost doubled since the 1980s, suggests a new study published in BJOG: An International Journal of Obstetrics and...

Clusters Of Congenital Anomalies Likely To Go Unnoticed Due To Lack Of Nationwide Surveillance

One baby in every 45 was born with a congenital anomaly in 2010 according to the second annual report by the British Isles Network of Congenital Anomaly Registers (BINOCAR), released today (Thursday)....

The number of multiple births affected by congenital anomalies has doubled since the 1980s

The number of congenital anomalies, or birth defects arising from multiple births has almost doubled since the 1980s, suggests a new study published today (6 February) in BJOG: An International Journa...

Congenital anomaly clusters may be going undetected in UK

A lack of national surveillance of congenital anomalies in England and Wales may lead to clusters of congenital conditions going unnoticed, say UK researchers.

Number of multiple births affected by congenital anomalies has doubled since the 1980s

The number of congenital anomalies, or birth defects arising from multiple births has almost doubled since the 1980s, suggests a new study.

Lack of nationwide surveillance may lead to clusters of congenital anomalies going unnoticed

One baby in every 45 was born with a congenital anomaly in 2010 according to the second annual report by the British Isles Network of Congenital Anomaly Registers (BINOCAR), released today (Thursday).

Magnets help steer ablation catheters in congenital heart disease

NEW YORK (Reuters Health) - Using tiny magnets in the tip and shaft of a catheter to steer it remotely, doctors are treating arrhythmias in patients with congenital heart disease -- a population i...

How it feels to withdraw feeding from newborn babies

The voice on the other end of the phone describes a newborn baby and a lengthy list of unexpected congenital anomalies. I have a growing sense of dread as I listen. The parents want “nothing done”...

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Congenital anomalies in the baboon (Papio spp.).

Background  A comprehensive survey of the prevalence of congenital anomalies in baboons has not been previously reported. We report the congenital anomalies observed over a 26-year period in a large...

Prenatal diagnosis of a fetus with anencephaly and thumb agenesis.

Severe anomalies of the forebrain together with reduction limb anomalies are a rare congenital anomalies association. We report a prenatal diagnosis of acalvaria, anencephaly and thumb agenesis in a v...

Imaging of congenital coronary artery anomalies.

Imaging of the coronary arteries is an important part of the evaluation of children with congenital heart disease and isolated congenital coronary artery anomalies. Echocardiography remains the main i...

Hereditary isolated ossicular anomalies in two generations of patients.

We present herein a report of an isolated form of ossicular anomaly that affected two generations of patients. Two female patients, a mother and daughter, were admitted with complaints of conductive h...

Novel association of multiple gastrointestinal anomalies in a single patient: Can Sonic Hedgehog explain it?

The occurrence of four gastrointestinal (GIT) anomalies in a single patient is extremely rare. Only one report of four GIT anomalies in a child has been published in the English literature. The curren...

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