Quelle est la durée du traitement par déferoxamine ?
La durée dépend de la gravité de la surcharge en fer, souvent plusieurs mois.
DéferoxamineDurée du traitementSurcharge en fer
#3
Peut-on combiner déferoxamine avec d'autres traitements ?
Oui, elle peut être combinée avec d'autres agents chélateurs selon les besoins.
DéferoxamineAgents chélateursTraitement combiné
#4
Quels sont les objectifs du traitement par déferoxamine ?
Réduire la surcharge en fer et prévenir les complications associées.
DéferoxamineSurcharge en ferComplications
#5
La déferoxamine est-elle efficace pour tous les patients ?
Son efficacité peut varier selon la cause de la surcharge en fer et la réponse individuelle.
DéferoxamineEfficacitéRéponse individuelle
Complications
5
#1
Quelles complications peuvent survenir avec une surcharge en fer ?
Les complications incluent des maladies cardiaques, des troubles hépatiques et endocriniens.
Surcharge en ferComplicationsMaladies cardiaques
#2
La déferoxamine peut-elle causer des complications ?
Oui, des complications comme des réactions allergiques et des troubles rénaux peuvent survenir.
DéferoxamineComplicationsRéactions allergiques
#3
Comment prévenir les complications liées à la surcharge en fer ?
Un traitement précoce et un suivi régulier des niveaux de fer sont essentiels.
PréventionSurcharge en ferSuivi régulier
#4
Quels sont les risques à long terme d'une surcharge en fer ?
Les risques incluent des dommages organiques permanents, notamment au cœur et au foie.
Surcharge en ferRisques à long termeDommages organiques
#5
La déferoxamine peut-elle réduire les complications ?
Oui, elle aide à réduire la surcharge en fer et donc à diminuer les complications associées.
DéferoxamineRéduction des complicationsSurcharge en fer
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Consanguineous marriage is defined as marriage between first or second-degree cousins, with high prevalence in many cultures and societies. Descendants from consanguineous unions have an increased ris...
Inherited cardiomyopathies are a prevalent cause of heart failure and sudden cardiac death. Both hypertrophic (HCM) and dilated cardiomyopathy (DCM) are genetically heterogeneous and typically present...
Drawing on interviews, autobiographies, and online ethnography, this paper explores the ways in which nonbiological lesbian parents and their family members use photographs to articulate their family ...
Hereditary blood diseases are widespread among the Arab population due to the high rates of consanguineous marriages; research regarding the perception of consanguineous marriage in some countries, su...
A cross-sectional study used a self-administered questionnaire among 395 Qatari adults aged 18-35 who attended primary healthcare institutions in Qatar. A convenience sampling technique was used to se...
Approximately 45% of the participants had a positive perception toward consanguineous marriage, and the most common reason stated by those participants was "habit and traditions." The prevalence of co...
The prevalence of consanguineous marriage is high among the Qatari population, and this requires an immediate need for community-based campaigns to raise public awareness about the problem and its pot...
The clinical utility of exome sequencing is now well documented. Rapid exome sequencing (RES) is more resource-intensive than regular exome sequencing and is typically employed in specialized clinical...
Here, we describe our experience with rapid exome sequencing (RES) in a highly consanguineous population. Clinical settings included intensive care units, prenatal cases approaching the legal cutoff f...
A positive molecular finding (a pathogenic or likely pathogenic variant that explains the phenotype) was observed in 80 of 189 cases (42%), while 15 (8%) and 94 (50%) received ambiguous (variant of un...
This work expands the diversity of environments in which RES has a demonstrable clinical utility....
Papillon-Lefevre syndrome (PLS) is a rare autosomal recessive syndrome, and consanguinity has been reported in 20%-40% of cases. It is characterised by palmoplantar hyperkeratosis associated with seve...
Consanguineous populations have a higher frequency of autosomal recessive diseases when compared to the rest of the world. This frequency is high enough that families in these populations may even hav...
Retinitis Pigmentosa (RP) is a clinically and genetically progressive retinal dystrophy associated with severe visual impairments and sometimes blindness, the most common syndromic form of which is Us...
Four consanguineous families of Pashtun ethnic group were investigated which were referred by the local collaborating ophthalmologists. In total 42 individuals in four families were recruited and inve...
Pathogenic gene variants were identified in all four families, including two in cone dystrophy and RP genes in the same family (PDE6C; c.480delG, p.Asn161ThrfsTer33 and TULP1; c.238 C > T, p.Gln80Ter)...
This study increases knowledge of the genetic basis of retinal dystrophies in families from Pakistan providing information important for genetic testing and diagnostic provision particularly from the ...
Split-hand/foot malformation (SHFM) with long-bone deficiency (SHFLD) is a rare condition characterized by SHFM associated with long-bone malformation usually involving the tibia. It includes three di...
Psychiatric disorders are characterized by alteration in emotions, mood and behavior. Genetics is known to play a significant role in the development of psychiatric disorders. Genome-wide association ...
We visited psychiatric outpatient departments of multiple hospitals in Lahore, Pakistan. We focused on psychosis, as it can occur in several DSM disorders such as schizophrenia, dementia and bipolar d...
We identified eight pedigrees with two or more psychotic individuals in each family. Clinical diagnoses determined by their psychiatrists included ten individuals with schizophrenia; four individuals ...
Our research highlights an alternative approach to discovery of rare recessively inherited genetic variants causing psychiatric disorders that have remained unidentified to date. These findings could ...