questionsmedicales.fr
Phénomènes génétiques
Structures génétiques
Chromosomes
Chromosomes de mammifère
Chromosomes humains
Chromosomes humains : Questions médicales fréquentes
Termes MeSH sélectionnés :
Diagnostic
5
Caryotype
Anomalies chromosomiques
Tests génétiques
Séquençage
Malformations congénitales
Retard de développement
Dépistage
Grossesse à risque
Échographie
Anomalies physiques
Symptômes
5
Syndromes chromosomiques
Retards mentaux
Troubles neurologiques
Anomalies physiques
Syndrome de Down
Tonus musculaire
Troubles du comportement
Difficultés d'apprentissage
Prévention
5
Conseils génétiques
Anomalies chromosomiques
Santé maternelle
Grossesse
Dépistage prénatal
Anomalies chromosomiques
Alimentation
Acide folique
Antécédents familiaux
Risque
Traitements
5
Thérapie génique
Recherche
Soins médicaux
Thérapies physiques
Interventions précoces
Éducation
Complications
5
Complications
Retards de développement
Fertilité
Anomalies chromosomiques
Maladies associées
Risque accru
Traitements médicaux
Interventions
Suivi médical
Complications à long terme
Facteurs de risque
5
Facteurs de risque
Âge maternel
Expositions environnementales
Radiations
Maladies génétiques
Antécédents familiaux
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"name": "Article complet : Chromosomes humains - Questions et réponses",
"headline": "Questions et réponses médicales fréquentes sur Chromosomes humains",
"description": "Une compilation de questions et réponses structurées, validées par des experts médicaux.",
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"name": "Diagnostic",
"headline": "Diagnostic sur Chromosomes humains",
"description": "Comment diagnostiquer une anomalie chromosomique ?\nQuels tests génétiques sont disponibles ?\nQuels signes indiquent un problème chromosomique ?\nQuand faire un test de dépistage chromosomique ?\nQuel rôle joue l'échographie dans le diagnostic ?",
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"name": "Symptômes",
"headline": "Symptômes sur Chromosomes humains",
"description": "Quels sont les symptômes des syndromes chromosomiques ?\nComment se manifestent les troubles liés aux chromosomes ?\nLes anomalies chromosomiques causent-elles des douleurs ?\nY a-t-il des symptômes spécifiques au syndrome de Down ?\nLes troubles chromosomiques affectent-ils le comportement ?",
"url": "https://questionsmedicales.fr/mesh/D002877?mesh_terms=Blood+Transfusion#section-symptômes"
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"name": "Prévention",
"headline": "Prévention sur Chromosomes humains",
"description": "Peut-on prévenir les anomalies chromosomiques ?\nQuel rôle joue la santé maternelle ?\nLes tests de dépistage prénatal sont-ils efficaces ?\nL'alimentation influence-t-elle les anomalies chromosomiques ?\nLes antécédents familiaux augmentent-ils les risques ?",
"url": "https://questionsmedicales.fr/mesh/D002877?mesh_terms=Blood+Transfusion#section-prévention"
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"name": "Traitements",
"headline": "Traitements sur Chromosomes humains",
"description": "Quels traitements existent pour les anomalies chromosomiques ?\nLa thérapie génique est-elle une option ?\nComment gérer les symptômes des syndromes chromosomiques ?\nLes médicaments peuvent-ils aider ?\nY a-t-il des interventions précoces recommandées ?",
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"name": "Complications",
"headline": "Complications sur Chromosomes humains",
"description": "Quelles complications peuvent survenir avec des anomalies chromosomiques ?\nLes anomalies chromosomiques affectent-elles la fertilité ?\nY a-t-il des risques de maladies associées ?\nLes complications peuvent-elles être traitées ?\nLes personnes atteintes ont-elles besoin de soins continus ?",
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},
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"name": "Facteurs de risque",
"headline": "Facteurs de risque sur Chromosomes humains",
"description": "Quels sont les facteurs de risque pour les anomalies chromosomiques ?\nL'âge des parents influence-t-il les risques ?\nLes expositions environnementales sont-elles un risque ?\nLes maladies génétiques augmentent-elles les risques ?\nLe mode de vie peut-il influencer les risques ?",
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"@type": "Question",
"name": "Comment diagnostiquer une anomalie chromosomique ?",
"position": 1,
"acceptedAnswer": {
"@type": "Answer",
"text": "Un caryotype est réalisé pour examiner le nombre et la structure des chromosomes."
}
},
{
"@type": "Question",
"name": "Quels tests génétiques sont disponibles ?",
"position": 2,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les tests incluent l'analyse de l'ADN, le caryotype et le séquençage génomique."
}
},
{
"@type": "Question",
"name": "Quels signes indiquent un problème chromosomique ?",
"position": 3,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des malformations congénitales, des retards de développement ou des troubles de la fertilité."
}
},
{
"@type": "Question",
"name": "Quand faire un test de dépistage chromosomique ?",
"position": 4,
"acceptedAnswer": {
"@type": "Answer",
"text": "Il est recommandé lors de grossesses à risque ou d'antécédents familiaux d'anomalies."
}
},
{
"@type": "Question",
"name": "Quel rôle joue l'échographie dans le diagnostic ?",
"position": 5,
"acceptedAnswer": {
"@type": "Answer",
"text": "L'échographie peut détecter des anomalies physiques pouvant indiquer des problèmes chromosomiques."
}
},
{
"@type": "Question",
"name": "Quels sont les symptômes des syndromes chromosomiques ?",
"position": 6,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les symptômes varient, incluant des retards mentaux, des malformations et des troubles comportementaux."
}
},
{
"@type": "Question",
"name": "Comment se manifestent les troubles liés aux chromosomes ?",
"position": 7,
"acceptedAnswer": {
"@type": "Answer",
"text": "Ils peuvent se manifester par des anomalies physiques, des problèmes de croissance ou des troubles neurologiques."
}
},
{
"@type": "Question",
"name": "Les anomalies chromosomiques causent-elles des douleurs ?",
"position": 8,
"acceptedAnswer": {
"@type": "Answer",
"text": "Elles ne causent pas directement de douleurs, mais peuvent entraîner des complications douloureuses."
}
},
{
"@type": "Question",
"name": "Y a-t-il des symptômes spécifiques au syndrome de Down ?",
"position": 9,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, incluant un visage plat, des yeux en amande et un tonus musculaire faible."
}
},
{
"@type": "Question",
"name": "Les troubles chromosomiques affectent-ils le comportement ?",
"position": 10,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certains peuvent entraîner des troubles du comportement ou des difficultés d'apprentissage."
}
},
{
"@type": "Question",
"name": "Peut-on prévenir les anomalies chromosomiques ?",
"position": 11,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines anomalies ne peuvent pas être prévenues, mais des conseils génétiques peuvent aider."
}
},
{
"@type": "Question",
"name": "Quel rôle joue la santé maternelle ?",
"position": 12,
"acceptedAnswer": {
"@type": "Answer",
"text": "Une bonne santé maternelle avant et pendant la grossesse peut réduire certains risques chromosomiques."
}
},
{
"@type": "Question",
"name": "Les tests de dépistage prénatal sont-ils efficaces ?",
"position": 13,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, ils peuvent détecter certaines anomalies chromosomiques avant la naissance."
}
},
{
"@type": "Question",
"name": "L'alimentation influence-t-elle les anomalies chromosomiques ?",
"position": 14,
"acceptedAnswer": {
"@type": "Answer",
"text": "Une alimentation équilibrée et des suppléments d'acide folique peuvent réduire certains risques."
}
},
{
"@type": "Question",
"name": "Les antécédents familiaux augmentent-ils les risques ?",
"position": 15,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des antécédents familiaux d'anomalies chromosomiques peuvent augmenter le risque de récurrence."
}
},
{
"@type": "Question",
"name": "Quels traitements existent pour les anomalies chromosomiques ?",
"position": 16,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les traitements varient selon les symptômes et peuvent inclure thérapies, chirurgie ou médicaments."
}
},
{
"@type": "Question",
"name": "La thérapie génique est-elle une option ?",
"position": 17,
"acceptedAnswer": {
"@type": "Answer",
"text": "La thérapie génique est en recherche pour certaines anomalies, mais n'est pas encore largement disponible."
}
},
{
"@type": "Question",
"name": "Comment gérer les symptômes des syndromes chromosomiques ?",
"position": 18,
"acceptedAnswer": {
"@type": "Answer",
"text": "La gestion inclut des soins médicaux, des thérapies physiques et des soutiens éducatifs."
}
},
{
"@type": "Question",
"name": "Les médicaments peuvent-ils aider ?",
"position": 19,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certains médicaments peuvent traiter des symptômes spécifiques comme l'anxiété ou l'hyperactivité."
}
},
{
"@type": "Question",
"name": "Y a-t-il des interventions précoces recommandées ?",
"position": 20,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des interventions précoces en éducation et en thérapie sont cruciales pour le développement."
}
},
{
"@type": "Question",
"name": "Quelles complications peuvent survenir avec des anomalies chromosomiques ?",
"position": 21,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les complications incluent des problèmes de santé chroniques, des retards de développement et des troubles mentaux."
}
},
{
"@type": "Question",
"name": "Les anomalies chromosomiques affectent-elles la fertilité ?",
"position": 22,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines anomalies peuvent entraîner des problèmes de fertilité chez les hommes et les femmes."
}
},
{
"@type": "Question",
"name": "Y a-t-il des risques de maladies associées ?",
"position": 23,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les personnes avec des anomalies chromosomiques peuvent avoir un risque accru de certaines maladies."
}
},
{
"@type": "Question",
"name": "Les complications peuvent-elles être traitées ?",
"position": 24,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines complications peuvent être gérées avec des traitements médicaux ou des interventions."
}
},
{
"@type": "Question",
"name": "Les personnes atteintes ont-elles besoin de soins continus ?",
"position": 25,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, un suivi médical régulier est souvent nécessaire pour gérer les complications à long terme."
}
},
{
"@type": "Question",
"name": "Quels sont les facteurs de risque pour les anomalies chromosomiques ?",
"position": 26,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les facteurs incluent l'âge maternel avancé, des antécédents familiaux et certaines expositions environnementales."
}
},
{
"@type": "Question",
"name": "L'âge des parents influence-t-il les risques ?",
"position": 27,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, l'âge avancé des parents, surtout de la mère, augmente le risque d'anomalies chromosomiques."
}
},
{
"@type": "Question",
"name": "Les expositions environnementales sont-elles un risque ?",
"position": 28,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines expositions, comme les radiations ou les produits chimiques, peuvent augmenter les risques."
}
},
{
"@type": "Question",
"name": "Les maladies génétiques augmentent-elles les risques ?",
"position": 29,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des antécédents de maladies génétiques dans la famille peuvent accroître le risque d'anomalies."
}
},
{
"@type": "Question",
"name": "Le mode de vie peut-il influencer les risques ?",
"position": 30,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des habitudes comme le tabagisme ou l'alcool peuvent augmenter le risque d'anomalies chromosomiques."
}
}
]
}
]
}
Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale
Validation scientifique effectuée le 31/03/2025
Contenu vérifié selon les dernières recommandations médicales
└─
Chromosomes humains 1-3
Chromosomes, Human, 1-3
D002900
-
G05.360.162.520.300.235
└─
Chromosomes humains 4-5
Chromosomes, Human, 4-5
D002905
-
G05.360.162.520.300.280
└─
Chromosomes humains 6-12 et X
Chromosomes, Human, 6-12 and X
D002906
-
G05.360.162.520.300.325
└─
Chromosomes humains 13-15
Chromosomes, Human, 13-15
D002901
-
G05.360.162.520.300.370
└─
Chromosomes humains 16-18
Chromosomes, Human, 16-18
D002902
-
G05.360.162.520.300.415
└─
Chromosomes humains 19-20
Chromosomes, Human, 19-20
D002903
-
G05.360.162.520.300.460
└─
Chromosomes humains 21-22 et Y
Chromosomes, Human, 21-22 and Y
D002904
-
G05.360.162.520.300.505
└─└─
Chromosomes humains de la paire 1
Chromosomes, Human, Pair 1
D002878
-
G05.360.162.520.300.235.240
└─└─
Chromosomes humains de la paire 2
Chromosomes, Human, Pair 2
D002889
-
G05.360.162.520.300.235.245
└─└─
Chromosomes humains de la paire 3
Chromosomes, Human, Pair 3
D002893
-
G05.360.162.520.300.235.250
└─└─
Chromosomes humains de la paire 4
Chromosomes, Human, Pair 4
D002894
-
G05.360.162.520.300.280.285
└─└─
Chromosomes humains de la paire 5
Chromosomes, Human, Pair 5
D002895
-
G05.360.162.520.300.280.290
└─└─
Chromosomes humains de la paire 6
Chromosomes, Human, Pair 6
D002896
-
G05.360.162.520.300.325.330
└─└─
Chromosomes humains de la paire 7
Chromosomes, Human, Pair 7
D002897
-
G05.360.162.520.300.325.335
└─└─
Chromosomes humains de la paire 8
Chromosomes, Human, Pair 8
D002898
-
G05.360.162.520.300.325.340
└─└─
Chromosomes humains de la paire 9
Chromosomes, Human, Pair 9
D002899
-
G05.360.162.520.300.325.345
└─└─
Chromosomes humains de la paire 10
Chromosomes, Human, Pair 10
D002879
-
G05.360.162.520.300.325.350
└─└─
Chromosomes humains de la paire 11
Chromosomes, Human, Pair 11
D002880
-
G05.360.162.520.300.325.355
└─└─
Chromosomes humains de la paire 12
Chromosomes, Human, Pair 12
D002881
-
G05.360.162.520.300.325.360
└─└─
Chromosomes humains de la paire 13
Chromosomes, Human, Pair 13
D002882
-
G05.360.162.520.300.370.375
└─└─
Chromosomes humains de la paire 14
Chromosomes, Human, Pair 14
D002883
-
G05.360.162.520.300.370.380
└─└─
Chromosomes humains de la paire 15
Chromosomes, Human, Pair 15
D002884
-
G05.360.162.520.300.370.385
└─└─
Chromosomes humains de la paire 16
Chromosomes, Human, Pair 16
D002885
-
G05.360.162.520.300.415.420
└─└─
Chromosomes humains de la paire 17
Chromosomes, Human, Pair 17
D002886
-
G05.360.162.520.300.415.425
└─└─
Chromosomes humains de la paire 18
Chromosomes, Human, Pair 18
D002887
-
G05.360.162.520.300.415.430
└─└─
Chromosomes humains de la paire 19
Chromosomes, Human, Pair 19
D002888
-
G05.360.162.520.300.460.465
└─└─
Chromosomes humains de la paire 20
Chromosomes, Human, Pair 20
D002890
-
G05.360.162.520.300.460.470
└─└─
Chromosomes humains de la paire 21
Chromosomes, Human, Pair 21
D002891
-
G05.360.162.520.300.505.510
└─└─
Chromosomes humains de la paire 22
Chromosomes, Human, Pair 22
D002892
-
G05.360.162.520.300.505.515
7 publications dans cette catégorie
Affiliations :
Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
6 publications dans cette catégorie
Affiliations :
Department of Biomolecular Engineering, University of California Santa Cruz, Santa Cruz, CA, USA.
UC Santa Cruz Genomics Institute, University of California Santa Cruz, Santa Cruz, CA, USA.
5 publications dans cette catégorie
Affiliations :
Genome Informatics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Publications dans "Chromosomes humains" :
5 publications dans cette catégorie
Affiliations :
Genome Informatics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Publications dans "Chromosomes humains" :
5 publications dans cette catégorie
Affiliations :
Stowers Institute for Medical Research, Kansas City, MO, USA.
University of Kansas Medical Center, Kansas City, MO, USA.
Publications dans "Chromosomes humains" :
5 publications dans cette catégorie
Affiliations :
Genome Informatics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA. adam.phillippy@nih.gov.
Publications dans "Chromosomes humains" :
5 publications dans cette catégorie
Affiliations :
Division of Genome and Cellular Functions, Department of Molecular and Cellular Biology, Faculty of Medicine, School of Life Science, Tottori University, 86 Nishi-cho, Yonago, Tottori, 683-8503, Japan. kazuki@tottori-u.ac.jp.
Chromosome Engineering Research Center, Tottori University, 86 Nishi-cho, Yonago, Tottori, 683-8503, Japan. kazuki@tottori-u.ac.jp.
Publications dans "Chromosomes humains" :
4 publications dans cette catégorie
Affiliations :
Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Publications dans "Chromosomes humains" :
4 publications dans cette catégorie
Affiliations :
Stowers Institute for Medical Research, Kansas City, MO, USA.
Publications dans "Chromosomes humains" :
4 publications dans cette catégorie
Affiliations :
Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Investigator, Howard Hughes Medical Institute, University of Washington, Seattle, WA, USA.
Publications dans "Chromosomes humains" :
4 publications dans cette catégorie
Affiliations :
Chromosome Engineering Research Center, Tottori University, 86 Nishi-cho, Yonago, Tottori, 683-8503, Japan.
Publications dans "Chromosomes humains" :
3 publications dans cette catégorie
Affiliations :
Department of Genetics, Genomics and Informatics, University of Tennessee Health Science Center, Memphis, TN, USA.
Publications dans "Chromosomes humains" :
3 publications dans cette catégorie
Affiliations :
Department of Genetics, Genomics and Informatics, University of Tennessee Health Science Center, Memphis, TN, USA.
Genomics Research Centre, Human Technopole, Milan, Italy.
Publications dans "Chromosomes humains" :
3 publications dans cette catégorie
Affiliations :
Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Publications dans "Chromosomes humains" :
3 publications dans cette catégorie
Affiliations :
Department of Data Sciences, Dana-Farber Cancer Institute, Boston, MA, USA.
Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Publications dans "Chromosomes humains" :
3 publications dans cette catégorie
Affiliations :
Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Publications dans "Chromosomes humains" :
3 publications dans cette catégorie
Affiliations :
Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Publications dans "Chromosomes humains" :
3 publications dans cette catégorie
Affiliations :
Developmental Therapeutics Branch, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.
Publications dans "Chromosomes humains" :
3 publications dans cette catégorie
Affiliations :
Division of Genome and Cellular Functions, Department of Molecular and Cellular Biology, Faculty of Medicine, School of Life Science, Tottori University, 86 Nishi-cho, Yonago, Tottori, 683-8503, Japan. narumi@toyaku.ac.jp.
Chromosome Engineering Research Center, Tottori University, 86 Nishi-cho, Yonago, Tottori, 683-8503, Japan. narumi@toyaku.ac.jp.
Laboratory of Bioengineering, Faculty of Life Sciences, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachiohji, Tokyo, 192-0392, Japan. narumi@toyaku.ac.jp.
Publications dans "Chromosomes humains" :
3 publications dans cette catégorie
Affiliations :
Department of Biochemistry and Biophysics, Graduate Program in Biochemistry and Molecular Biophysics, and Epigenetics Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Publications dans "Chromosomes humains" :
Using a large national database, we evaluated the relationship between RBC transfusion volume, RBC transfusion rate, and in-hospital mortality to explore the presence of a futility threshold in trauma...
The ACS-TQIP 2013 to 2018 database was analyzed. Adult patients who received ultramassive blood transfusion (≥20 units of RBC/24 hours) were included. RBC transfusion volume and rate were captured at ...
Among 5,135 patients analyzed, in-hospital mortality rate was 62.1% (n = 3,190), and 4-hour and 24-hour mortality rates were 17.53% (n = 900) and 42.41% (n = 2,178), respectively. RBC transfusion volu...
RBC transfusion volume within 4 or 24 hours and mean RBC transfusion rate within 4 hours were not markers of futility. The observed maximum length of survival per mean RBC transfusion rate could infor...
Whole blood is gaining popularity in the treatment of traumatic massive haemorrhage. The prospective study of Hazelton et al. in 2022 shows that mortality is reduced in patients treated with whole blo...
Autoimmune rheumatic disorders (ARD) represent a wide spectrum of disorders that affect in priority the joints, bones, muscles, and connective tissues. Examples of ARD include rheumatoid arthritis, sy...
The scant evidence on the use of transfusions in neonatal care explains the limitations of current clinical guidelines. Despite this, in this document we explore the most recent evidence to make recom...
Data demonstrate the benefit of blood product administration near point-of-injury (POI). Fresh whole blood transfusion from a pre-screened donor provides a source of blood at the POI when resources ar...
We conducted a prospective, observational study of medics with varying levels of experience. Inexperienced medics were those with minimal or no reported experience learning the autologous transfusion ...
The median number of attempts for inexperienced and experienced medics was 1 versus 1 (interquartile range 1-1 for both, p = .260). The inexperienced medics had a slower median time to needle venipunc...
Inexperienced medics have longer procedure times when training autologous whole blood transfusion skills. This data will help establish training measures of performance for skills optimization when le...
Whether clinical practice guidelines have a significant impact on practice is unclear. The effect of guideline recommendations on clinical practice often a lags behind the date of publication. We eval...
RhD-negative blood products are in chronic short supply leading to renewed interest in utilizing RhD-positive blood products for emergency transfusions. This study assessed parental perceptions of eme...
A survey of parents/guardians was conducted on their tolerance of transfusing RhD-positive blood to RhD-negative female children ≤17 years old at four level 1 pediatric hospitals....
In total, 621 parents/guardians were approached of whom 378/621 (61%) completed the survey in its entirety and were included in the analysis. Respondents were mostly females [295/378 (78%)], White [24...
Most parents were willing to accept RhD-positive blood products on behalf of RhD-negative female children in an emergency situation. Further discussions and evidence-based guidelines on transfusing Rh...
Repeated red blood cell (RBC) transfusions in preterm neonates cause the progressive displacement of fetal hemoglobin (HbF) by adult hemoglobin. The ensuing increase of oxygen delivery may result at t...
Blood transfusions are essential to treating anaemia of burn injuries. It has recently been observed that patients with non-major burns < 20%TBSA may also develop anaemia requiring transfusion of bloo...
To determine risk factors for transfusion of blood products in patients with non-major burn injuries and assess transfusion practices to establish impact on patient outcome....
Our study included 182 adult patients with non-major burn injuries, < 20%TBSA admitted over a 3-year period at the Department of Plastic Surgery and Burns Unit of the Emergency County Hospital Cluj-Na...
37.9% of patients included in our study developed anaemia throughout admission and 7.7% underwent blood transfusions. Mean Hb levels triggering blood transfusions have been recorded at 7.4 (IQR=8.8-9....
Patient related comorbidities correlate with higher transfusion rates in non-major burn injuries. Due to the risk associated with the use of blood products decision to transfuse should adhere to curre...
Sc1 is a high-prevalence blood group antigen that is part of the Scianna blood group system. The clinical significance of Scianna antibodies is not well understood because of their rarity; there are o...