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Published in 2022 at "AORN journal"
DOI: 10.1002/aorn.13712
Abstract: Down syndrome (DS) is the most common chromosomal abnormality in humans that is compatible with life. This syndrome occurs when there is an extra copy of the 21st chromosome. Down syndrome is associated with numerous…
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Keywords:
review key;
syndrome review;
key perioperative;
patient ... See more keywords
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1
Published in 2018 at "Journal of the science of food and agriculture"
DOI: 10.1002/jsfa.9115
Abstract: Metabolic syndrome is one of the rising global health problems and medical challenges due to several clinical complications it may cause, for example increasing the risk of myocardial infarction and hypertension. However, great attention has…
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Keywords:
syndrome review;
silymarin metabolic;
effects silymarin;
metabolic syndrome ... See more keywords
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Published in 2021 at "Current problems in cardiology"
DOI: 10.1016/j.cpcardiol.2021.100937
Abstract: Brugada syndrome (BrS) is characterized by ventricular arrhythmias in patients without structural cardiac alteration. Some patients present repeated episodes of ventricular tachycardia. Epicardial catheter ablation makes it possible to decrease arrhythmic recurrence in these patients.
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Keywords:
syndrome review;
brugada syndrome;
two cases;
review two ... See more keywords
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Published in 2022 at "Journal of Hypertension"
DOI: 10.1097/hjh.0000000000003321
Abstract: Acquired cardiovascular diseases account for much of the increased risk of premature death in patients with Turner syndrome (TS). Hypertension is a major modifiable cardiovascular risk factor. It has a high prevalence in TS developing…
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Keywords:
syndrome review;
turner syndrome;
hypertension;
hypertension turner ... See more keywords
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Published in 2019 at "Clinical Dysmorphology"
DOI: 10.1097/mcd.0000000000000301
Abstract: Klippel-Feil syndrome is a congenital defect in the formation or segmentation of the cervical spine. A wide spectrum of associated anomalies may be present. This heterogeneity has complicated clarification of the genetic causes and management…
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Keywords:
klippel feil;
syndrome review;
etiology;
feil syndrome ... See more keywords
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Published in 2021 at "Dermatologic Therapy"
DOI: 10.1111/dth.15082
Abstract: H syndrome is a rare autosomal recessive disorder with clinical features comprising: hyperpigmentation, hypertrichosis, hearing loss, heart anomalies, low height, hypogonadism and hepatosplenomegaly. H syndrome results from loss‐of‐function mutations in SLC29A3 which leads to abnormal…
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Keywords:
phenotypic variability;
syndrome review;
treatment options;
variability ... See more keywords
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Published in 2021 at "Journal of the European Academy of Dermatology and Venereology"
DOI: 10.1111/jdv.17226
Abstract: Netherton syndrome (NS) is an autosomal recessive ichthyosis with a broad range of extracutaneous manifestations, including faltering growth, rendering it a complex multisystem disease. Exploring longitudinal data on complications/comorbidities holds potential to reduce morbidity and…
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Keywords:
characteristics children;
syndrome review;
dermatology;
review patients ... See more keywords
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Published in 2022 at "BMJ Case Reports"
DOI: 10.1136/bcr-2022-249414
Abstract: A woman in her 20s, symptomatic since the age of 4 with short stature, hearing loss, skin hyperpigmentation and induration over the medial aspect of the thigh, hypertrichosis, histiocytes on biopsy, lymphadenopathy, dilated scleral vessels,…
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Keywords:
syndrome review;
review rheumatological;
report syndrome;
case report ... See more keywords
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Published in 2023 at "Journal of Investigative Medicine High Impact Case Reports"
DOI: 10.1177/23247096221150631
Abstract: Wolfram syndrome (WS) is a rare genetic disorder typically characterized by juvenile onset diabetes mellitus, optic atrophy, hearing loss, diabetes insipidus, and neurodegeneration. There would be a high index of clinical suspicion for WS when…
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Keywords:
syndrome review;
review literature;
siblings wolfram;
pair siblings ... See more keywords
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Published in 2022 at "Radiologia Brasileira"
DOI: 10.1590/0100-3984.2021.0010
Abstract: Moyamoya disease is a chronic occlusive cerebrovascular disease that is non-inflammatory and non-atherosclerotic. It is characterized by endothelial hyperplasia and fibrosis of the intracranial portion of the carotid artery and its proximal branches, leading to…
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Keywords:
syndrome review;
disease;
etiology;
moyamoya disease ... See more keywords
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Published in 2023 at "Life"
DOI: 10.3390/life13030809
Abstract: Sweet syndrome (SS) is a rare disease described as a febrile neutrophilic dermatosis with acute onset, the pathogenesis of which has not yet been elucidated. The syndrome is characterized by the sudden onset of erythematous…
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Keywords:
sweet syndrome;
syndrome review;
syndrome associated;
syndrome ... See more keywords