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Cardiac malformations
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Left-sided lesions (LSLs) account for an important fraction of severe congenital cardiovascular malformations (CVMs). The genetic contributions to LSLs are complex, and the mutations that cause these malformations span several diverse biological signaling pathways: TGFB, NOTCH, SHH, and more.
10p
vioraclene
31-03-2024
8
2
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Part 1 book "Feline cardiology" includes content: Heart murmurs and gallop heart sounds, exercise intolerance and syncope; pleural effusion; dyspnea and cough; cardiopulmonary arrest and cardiopulmonary cerebral resuscitation, radiography; echocardiography; cardiac biomarkers; electrocardiography; congenital heart malformations; hypertrophic cardiomyopathy; restrictive unclassified cardiomyopathy; dilated cardiomyopathy; arrhythmogenic right ventricular cardiomyopathy; cardiac neoplasia; miscellaneous myocardial disease.
205p
oursky10
04-12-2023
5
3
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Intracranial hemorrhage, including subarachnoid hemorrhage (SAH), is associated with many cardiac effects, including cardiac rhythm abnormalities, ischemic electrocardiographic (ECG) changes, elevated cardiac troponin levels, and regional wall motion abnormalities on echocardiogram.
6p
viwhitewolf
03-07-2023
4
2
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Loss of proprotein convertase subtilisin/kexin type 5 (Pcsk5) results in multiple developmental anomalies including cardiac malformations, caudal regression, pre-sacral mass, renal agenesis, anteroposterior patterning defects, and tracheo-oesophageal and anorectal malformations, and is a model for VACTERL/caudal regression/Currarino syndromes (VACTERL association - Vertebral anomalies, Anal atresia, Cardiac defects, Tracheoesophageal fistula and/or Esophageal atresia, Renal & Radial anomalies and Limb defects).
10p
viwyoming2711
16-12-2020
11
1
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13q33–q34 microdeletions are rare chromosomal aberrations associated with a high risk of developmental disability, facial dysmorphism, cardiac defects and other malformation of organs. It is necessary to collect and report evidence of this rare chromosome mutation to improve the prognosis of this rare disease.
6p
vimanama2711
28-07-2020
13
2
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Tuberous sclerosis complex (TSC) is an autosomal-dominant tumor suppressor gene syndrome that is characterized by the development of distinctive benign tumors and malformations in multiple organ systems (N Eng J Med 355:1345-1356, 2006).
5p
vichengna2711
25-02-2020
15
1
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Congenital heart disease (CHD) is the most prevalent congenital malformation affecting 1 in 100 newborns. While advances in early diagnosis and postnatal management have increased survival in CHD children, worrying long-term outcomes, particularly neurodevelopmental disability, have emerged as a key prognostic factor in the counseling of these pregnancies.
10p
vidublin2711
13-01-2020
28
1
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(BQ) Part 2 of the document Cerebral angiography normal anatomy and vascular pathology presents the following contents: Vascular malformations of the central nervous system, dural arteriovenous fistulas, arteriovenous fistulas, ischemic stroke, spontaneous dissection of carotid and vertebral arteries,...
205p
thangnamvoiva4
01-07-2016
51
3
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Congenital heart defects occur in approximately 1% of newborns and are a major cause of morbidity and mortality in infants and children. Many adult cardiac diseases also have developmental basis, such as heart valve malformations, among others. Therefore, dissecting the developmental and molecular mechanisms underlying such defects in embryos is of great importance in prevention and developing therapeutics for heart diseases that manifest in infants or later in adults.
356p
thienbinh1311
13-12-2012
51
4
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For much of the early history of medicine, the heart was considered to be the most sacred and mystical of all human organs. As a General Pediatrician, I tend to expect that the children I care for will have strong, properly functioning hearts. However, in situations where the heart is congenitally malformed or affected by inflammation or myopathy, it is reassuring and important to have a pediatric cardiologist and cardiac surgeon at my side to help me with decisions about further diagnostic testing and imaging, instituting medical therapy, and assessing the need for surgical intervention....
382p
bachduong1311
10-12-2012
65
6
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As one ascends rapidly to 3000 m (~10,000 ft), the reduction of the O 2 content of inspired air (FIO2) leads to a decrease in alveolar PO2 to about 60 mmHg, and a condition termed high-altitude illness develops (see above). At higher altitudes, arterial saturation declines rapidly and symptoms become more serious; and at 5000 m, unacclimatized individuals usually cease to be able to function normally.
5p
ongxaemnumber1
29-11-2010
82
3
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