174 results match your criteria: "Hospital de Pediatría SAMIC "Prof Dr Juan P Garrahan"[Affiliation]"

There exists a need to research new diagnostic and therapeutic approaches that consider hemolytic disease of fetus and newborn (HDFN)'s physiopathology and focus not only on the pregnant person's immune system but also on the fetal immune system. This implies, in the final sense, to view the fetus as our patient. In spite of having found a safe and efficient method of prevention of HDFN more than 50 years ago, HDFN continues to be a relevant cause of perinatal morbidity and mortality, due to lack of access to immunoprophylaxis.

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High-dose methotrexate is an effective and safe therapy. It is included in the treatment regimens of various hematologic and oncologic diseases. The acute and severe toxicity of this chemotherapeutic agent is unusual.

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Background: Shiga toxin-producing Escherichia coli-associated hemolytic uremic syndrome (STEC-HUS) is a severe condition mainly affecting children. It is one of the leading causes of acute kidney injury in the pediatric population. There is no established therapy for this disease.

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Introduction. Arboviruses, such as dengue and chikungunya, have caused multiple epidemics in the Americas. They are transmitted through mosquito bites; Aedes aegypti is their main vector.

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Neurofibromatosis type 1 (NF1) is the most common neurocutaneous disease. It is characterized by café-au-lait spots, melanocytic hamartomas of the iris, pseudo-freckles, neurofibromas, and tumor predisposition. The presence of neurofibromas in the thyroid gland is extremely rare.

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  • - Systemic lupus erythematosus (SLE) is a serious autoimmune disease that can affect multiple systems in the body, and while cardiovascular issues are common, aneurysms and aortic dissection are rare but deadly complications.
  • - A case study details a 16-year-old girl with SLE who experienced severe chest pain, leading to imaging that revealed a dilated aortic arch and a descending aortic aneurysm, despite no initial signs of cardiovascular disease.
  • - Unfortunately, after starting antihypertensive treatment and a Valsalva maneuver, the patient suffered an aneurysmal rupture and died within 12 hours, emphasizing the need to consider these serious complications when a patient with SLE presents with
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  • Vitamin A deficiency can lead to serious eye problems and is often linked to selective eating habits in children with autism spectrum disorder (ASD).
  • A study involving 13 children showed that many had significant neurological issues and obesity-related conditions due to low Vitamin A levels, with 61.5% of them also diagnosed with ASD.
  • Early identification of nutrient deficiencies through examining food intake is crucial for neuro-diverse children, as timely Vitamin A treatment can prevent long-term damage, including severe vision loss.
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Introduction. Hypoxic-ischemic encephalopathy (HIE) caused by lack of oxygen and perfusion to the brain can lead to acute neurological damage in newborns. Therapeutic hypothermia (TH) is the most effective and safest treatment.

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Childhood-onset systemic lupus erythematosus (cSLE) is a multisystem disease; its severity depends on the organs involved. Monogenic diseases have been described as predisposing to the onset of cSLE. Analytical and immunological tests are used for diagnostic confirmation.

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Introduction. Hypercalcemia is infrequent in pediatrics, of diverse etiology, and with multiorgan morbidity. Objective.

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Argentine and World Health Organization head circumference standards: A comparison study.

Arch Argent Pediatr

December 2024

Fundación Centro de Salud e Investigaciones Médicas (CESIM), Santa Rosa, Argentina. National Scientific and Technical Research Council (Consejo Nacional de Investigaciones Científicas y Técnicas, CONICET), City of Buenos Aires, Argentina.

Introduction. Several studies have shown population differences in head circumference (HC) that question the universal validity of the World Health Organization (WHO) standard to assess head growth. Objectives.

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ABCD syndrome (ABnormal Calcium, Calcinosis, and Creatinine in Down syndrome) is characterized by an association of hypercalcemia, hypercalciuria, nephrocalcinosis, and impaired kidney function in patients with Down syndrome. Only 7 cases have been published worldwide, although it is believed to be underdiagnosed. This report describes 2 new patients with ABCD syndrome and compares them with the cases reported to date.

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Introduction. Therapeutic hypothermia (TH) reduces the risk of death or disability in children with moderate to severe hypoxic ischemic encephalopathy (HIE). Objective.

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Argentine reference charts for head circumference from birth to 19 years of age.

Arch Argent Pediatr

October 2024

Fundación Centro de Salud e Investigaciones Médicas (CESIM), Santa Rosa, Argentina. National Scientific and Technical Research Council (Consejo Nacional de Investigaciones Científicas y Técnicas, CONICET), City of Buenos Aires, Argentina.

Introduction. Head circumference (HC) is an indicator of brain growth; growth charts are necessary to determine normal or pathological variations. Objectives.

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Introduction. Autism spectrum disorder (ASD) is characterized by difficulties in social communication and repetitive and stereotyped behaviors. In addition to the diagnostic category, the activities performed by children and adolescents and their social involvement are the main aspects to be considered according to the International Classification of Functioning, Disability, and Health (ICF) proposed by the World Health Organization to describe health status.

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  • XIAP deficiency is a rare genetic immune disorder linked to mutations in the XIAP gene, often diagnosed through flow cytometry to detect the absence of XIAP protein.
  • To enhance diagnostics, researchers explored how specifically stimulating leukocytes with L18-muramyl Di-Peptide (a NOD2 agonist) impacts the down-regulation of the L-selectin molecule, providing insights into XIAP functionality.
  • The study found that neutrophils and monocytes from XIAP-deficient patients exhibited significantly reduced CD62-L response to L18-MDP compared to healthy controls, indicating a dysfunction in the NOD2-XIAP signaling pathway, while the response to lipopolysaccharide was normal.
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Feeding difficulties in childhood: A narrative review.

Arch Argent Pediatr

October 2024

Degree of Nutrition, School of Medical Sciences, Pontificia Universidad Católica Argentina, Buenos Aires, Argentina.

It has been estimated that between 25% and 40% of healthy children show symptoms of feeding difficulties (FDs) during their growth and development; many times, these are not adequately diagnosed. The objective of this study was to conduct a narrative review that collected the available information on feeding difficulties. Assessment and management algorithms were developed based on the bibliographic evidence.

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  • A case study describes a young girl with asymptomatic subcutaneous nodules and high eosinophil levels, diagnosed with Wells' syndrome through histopathological examination.
  • After initial treatment with corticosteroids, which resulted in improvement, the recurrence of symptoms led to the use of dapsone as a second-line therapy, showing positive results.
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The study of central nervous system (CNS) tumors is a subject of great interest and such knowledge is of great importance in medical practice. The classifications of CNS neoplasms began in the mid-19th century, until the World Health Organization (WHO) published, in 1979, the first edition of a useful systematic review for the purpose of establishing a common language for all medical specialties. To date, 5 updated editions of neoplastic taxonomy have been published.

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Scurvy is a disease caused by vitamin C deficiency. Although rare, in recent years, the number of scurvy cases in children with eating disorders has increased. Its manifestations are varied because vitamin C is a cofactor in numerous processes, such as collagen synthesis.

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Introduction. Central venous catheter (CVC)-related infection is the main complication observed in patients undergoing hemodialysis with this type of venous access. Objective.

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