[National survey of pediatric residences in Argentina].

abstract：INTRODUCTION:Early excision has considerably improved outcome in extensive burns, but massive resections usually mean copious bleeding that must be conveniently corrected. The purpose of this study was to measure blood component use during escharectomies in children. MATERIAL AND METHODS:All pediatric patients with ac...

journal_title：Archivos argentinos de pediatria

authors： Julia AR,Basílico H,Magaldi G,Demirdjian G

更新日期：2010-02-01 00:00:00

abstract：:Food allergy poses a major problem during childhood. Component-resolved diagnosis detects allergy to proteins isolated in food. This descriptive study analyzes the use of customized and standardized recommendations in a sample made up of 22 children aged 2 to 16 years old with plant food allergy and assesses sensitivi...

journal_title：Archivos argentinos de pediatria

authors： Villarreal Balza De Vallejo O,Velasco Azagra M,López Picado A,Bernedo Belar N,Uriel Villate O,Frías Jiménez M,Audicana Berasategui M,Muñoz Lejarazu D,Arruti Oyarzabal N,Girao Popolizio IN,Martínez Arcediano A

更新日期：2015-12-01 00:00:00

abstract：:Health care providers' involvement is critical for quality of care improvement. Nevertheless, most residency programs do not include this topic. The objective is to describe an educational experience on quality of care improvement for residents. The development of an improvement cycle was included in the second year s...

journal_title：Archivos argentinos de pediatria

authors： Carozza Colombini MN,Silva C,Luiz Passarela M,Arzelan Clerici C,Llera J

更新日期：2020-08-01 00:00:00

abstract：OBJECTIVE:To determine the frequency of the MEFV gene mutations in pediatric patients diagnosed with HSP and to assess the effect of the MEFV gene mutations on their prognosis. Material and Methods. Ccross-sectional study; pediatric patients between 2-11 years diagnosed with HSP were included. These cases were investig...

journal_title：Archivos argentinos de pediatria

authors： Can E,Kılınç Yaprak Z,Hamilçıkan Ş,Erol M,Bostan Gayret Y Özgül Yiğit Ö

更新日期：2018-06-01 00:00:00

abstract：:Propionic acidemia is a rare metabolic disease (prevalence 1/100,000) that can be early detected with the newborn metabolic screening within the first 72 hours of life. It can have a severe neonatal presentation, a late intermittent onset or a chronic and progressive course. The treatment in the crisis consists in inv...

journal_title：Archivos argentinos de pediatria

authors： Félez Moliner I,Baquedano Lobera I,Navarro Rodríguez-Villanueva A,García Jiménez C

更新日期：2020-02-01 00:00:00

abstract：INTRODUCTION:Physicians' empathy is an advantage for a better patient care and resolution of disease, and is considered a relevant part of professional training. OBJECTIVE:To measure the level of empathy and its components in medical students of the city of Córdoba, Argentina. METHODS:This was an exploratory, cross-s...

journal_title：Archivos argentinos de pediatria

authors： Ulloque MJ,Villalba S,Varela de Villalba T,Fantini A,Quinteros S,Díaz-Narváez V

更新日期：2019-04-01 00:00:00

abstract：OBJECTIVE:To determine vitamin A content in breast milk and evaluate whether it satisfies the recommendations for infants. MATERIAL AND METHODS:Observational, prospective, cross sectional study. Milk samples were obtained between 30 and 90 days postpartum from mothers seen in public hospitals, and analyzed. Vitamin A ...

journal_title：Archivos argentinos de pediatria

authors： Matamoros N,Visentin S,Ferrari G,Falivene M,Fasano V,González HF

更新日期：2018-04-01 00:00:00

abstract：:The pediatrician is the best-informed professional to whom many families look to be the expert, not only on childhood illnesses but also on development. Early identification, diagnosis and monitoring of these patients are a real challenge for physicians who serve children. This guide provides recommendations for devel...

journal_title：Archivos argentinos de pediatria

authors： Comité de Crecimiento y Desarrollo.

更新日期：2017-06-01 00:00:00

abstract：INTRODUCTION:In 1999, the American Academy of Pediatrics (AAP) recommended perform a renal ultrasonography and avoiding cystourethrography to all infants between 2 and 24 months of age after their first urinary tract infection (UTI). In 2011, the AAP restricted voiding cystourethrography to children with a pathological...

journal_title：Archivos argentinos de pediatria

authors： Capone MA,Balestracci A,Toledo I,Martin SM

更新日期：2016-04-01 00:00:00

abstract：:Central diabetes insipidus is a rare disease in children caused by a deficiency of vasopressin. Its main clinical manifestations are polyuria and polydipsia. Brain malformations are one of the main causes. Desmopressin is the synthetic drug of choice for the treatment. One of the routes of administration is sublingual...

journal_title：Archivos argentinos de pediatria

authors： Marín GR,Baspineiro B,Vilca I

更新日期：2018-02-01 00:00:00

abstract：INTRODUCTION:Children take years to learn symbolic arithmetic. Nevertheless, such as animals and human adults, infants and children can represent approximate number in arrays of objects and sequences of events, and use these capacities to perform approximate addition and subtraction. OBJECTIVE:To evaluate whether pres...

journal_title：Archivos argentinos de pediatria

authors： Martínez J,Argibay PF

更新日期：2011-10-01 00:00:00

abstract：Introduction:Infant mortality comprises deaths among infants younger than one year old. The proportion of sudden unexpected death in infancy (SUDI) varies by country and based on the cause of death. Objective:To describe the spatial and temporal variation of SUDI in Argentina between 1991 and 2014 according to the Int...

journal_title：Archivos argentinos de pediatria

authors： Chapur VF,Alfaro EL,Bronberg R,Dipierri JE

更新日期：2019-06-01 00:00:00

abstract：:Trichorhinophalangeal syndrome type II (TRPSII) (synonym: Langer-Giedon syndrome) is a rare autosomal dominant contiguous gene syndrome, resulting from a microdeletion encompassing the EXT1 and the TRPS1 gene at 8q24 (MIM#150230). This syndrome combines the clinical features of two autosomal dominant disorders, tricho...

journal_title：Archivos argentinos de pediatria

authors： Hazan F,Korkmaz HA,Yararbaş K,Wuyts W,Tükün A,Collaborator.

更新日期：2016-12-01 00:00:00

abstract：:Anemia is very common in infants. Although its causes are usually not severe and treatable, proper etiologic diagnosis should be established. When anemia is non-regenerative, it can be caused by aplastic anemia, myelodysplastic syndrome, bone marrow infiltration or hematopoietic factors deficiencies. Another possible ...

journal_title：Archivos argentinos de pediatria

authors： Martínez de Zabarte Fernández JM,Rodríguez-Vigil Iturrate C,Martínez Faci C,García Jiménez I,Murillo Sanjuan L,Muñoz Mellado A

更新日期：2017-02-01 00:00:00

abstract：INTRODUCTION:Cystic fibrosis is a genetic autosomal recessive disease that affects approximately 1:6000 live births in our country. Chronic infection with Pseudomonas aeruginosa (PA) is associated with higher morbidity and-mortality, and deterioration of lung function. Treatment of initial infection is important to pre...

journal_title：Archivos argentinos de pediatria

authors： Giugno H,Castaños C,Lubatti A,Pinheiro JL,Hernández C,González Pena H

更新日期：2010-04-01 00:00:00

abstract：:Congenital erythropoietic porphyria is an extremely rare, autosomal recessive, non-acute cutaneous porphyria, caused by uroporphyrinogen III synthase deficiency, codificated by UROS gene on the chromosome 10q26.2. Porphyrins deposit in cornea, bones and teeth. The first symptoms could be manifested in early childhood,...

journal_title：Archivos argentinos de pediatria

authors： Salomone B C,Ogueta C I,Reyes V C,Durán S G,Aguirre N,Wietstruck A

更新日期：2018-04-01 00:00:00

abstract：:The environmental influence on human development can be studied by assessing similarities and discrepancies in developmental traits between biological and adopted siblings and twins, reared together and reared apart. Approximately 50% of total variance of general cognitive ability in a given population can be explaine...

journal_title：Archivos argentinos de pediatria

authors： Lejarraga H

更新日期：2010-12-01 00:00:00

abstract：:Phelan McDermid Syndrome is caused by the loss of genetic material in a chromosome from pair 22, at the band q13.3. We describe five patients with deletion 22q13.3 in order to establish a genotype-phenotype association, and report the first case described in conjoined twins. We analyzed the perinatal history, psychomo...

journal_title：Archivos argentinos de pediatria

authors： Canonero I,Montes C,Sturich A,Boterón M,Asinari M,Cuestas E,Rossi N

更新日期：2012-05-01 00:00:00

abstract：:Smith-Magenis syndrome (SMS) is characterized by distinctive facial features that progress with age, developmental delay, cognitive impairment, and behavioral abnormalities associated with molecular anomaly in 17p11.2. Treatment includes: early childhood intervention programs, special education, vocational training la...

journal_title：Archivos argentinos de pediatria

authors： Bronberg R,Ziembar M,Drut M,Goldschmidt E

更新日期：2008-04-01 00:00:00

abstract：INTRODUCTION:Valvular dysfunction secondary to obstruction of proximal catheter is relatively frequent at emergency room. However non-infectius obstruction of distal catheter is exceptional. CASE REPORT:A 6-year-old boy with dysfunction shunt due to migration of the abdominal catheter into the right scrotum. The patie...

journal_title：Archivos argentinos de pediatria

authors： Rivero-Garvía M,Barbeito Gaído JL,Morcillo J,Márquez Rivas J

更新日期：2013-01-01 00:00:00

abstract：:Dengue is a mosquito-borne viral disease, with worldwide distribution in tropical and subtropical areas. Argentina was certified free of Aedes aegypti in the sixties, however the vector reappered in 1984. In the nineties, small dengue outbreaks occurred with autocthonus diseases at first limited to the northern provin...

journal_title：Archivos argentinos de pediatria

authors： Berberian G,Fariña D,Rosanova MT,Hidalgo S,Enría D,Mitchenko A,Moreno J,Sánchez Soto I

更新日期：2011-06-01 00:00:00

abstract：:Posterior reversible encephalopathy is a rare disease in children. Clinical manifestations include headache, seizures, visual disturbances and altered consciousness associated with typical magnetic resonance images of the nervous system. The syndrome usually manifests in patients with eclampsia, solid organ transplant...

journal_title：Archivos argentinos de pediatria

authors： Marín GR

更新日期：2015-10-01 00:00:00

abstract：:The acid-labile subunit (ALS) is an 85 kDa glycoprotein that belongs to the leucine-rich repeat superfamily. It mainly circulates in serum bound to a high molecular weight ternary complex. The main and most widely studied function of ALS is to prolong the half-life of the binary complex formed by insulin-like growth f...

journal_title：Archivos argentinos de pediatria

authors： Zaidman VE

更新日期：2017-08-01 00:00:00

abstract：:X-linked agammaglobulinemia is a primary humoral immunodeficiency. It is a recessive X-linked disorder characterized by low or absent circulating mature B cells, hypo/agammaglobulinemia and no humoral response to immunizations due to mutations along chromosome X. It is characterized by severe, recurrent and difficult ...

journal_title：Archivos argentinos de pediatria

authors： Vera Sáez-Benito MC,López Úbeda M,Madurga Revilla P,de Arriba Muñoz A,Bustillo Alonso M,Rodríguez-Vigil Iturrate C

更新日期：2016-12-01 00:00:00

abstract：:Kidney disease is a global public health problem; affects more than 750million persons worldwide. The burden of kidney disease varies substantially across the world, as does its detection and treatment. Emerging evidence suggests that developing countries have a similar or even greater kidney disease burden than devel...

journal_title：Archivos argentinos de pediatria

authors： Crews DC,Bello AK,Saadi G

更新日期：2019-06-01 00:00:00

abstract：:Pubertal gynecomastia is a common concern in the consultation of the adolescent. Usually, it is accompanied by an emotional component that can lead to changes in everyday attitudes of youth. The responsability of the pediatrician is to rule out other etiologies, to avoid unnecessary additional studies, to limit active...

journal_title：Archivos argentinos de pediatria

authors： Comité Nacional de Endocrinología.

更新日期：2011-08-01 00:00:00

abstract：:The septo-optic dysplasia or De Morsier syndrome is an unusual disorder of the embryonic development. It consists of hypoplasia in one or both optic nerves, midline cerebral malformations and hypothalamic-pituitary dysfunction, which is inconstant. The present work describes the findings of 9 patients with septo-optic...

journal_title：Archivos argentinos de pediatria

authors： Zimmermann-Paiz MA,Fang-Sung JW

更新日期：2009-12-01 00:00:00

abstract：INTRODUCTION:The shift of adolescents from a pediatric to an adult health care facility is a complex process. The objective of this study was to assess the transition/transfer process for adolescents with chronic diseases at Hospital Garrahan. METHODS:Observational, cross-sectional, qualitative-quantitative study. Ret...

journal_title：Archivos argentinos de pediatria

authors： González F,Rodríguez Celin MLM,Roizen M,Mato R,García Arrigoni P,Ugo F,Staciuk R,Fano V

更新日期：2017-12-01 00:00:00

abstract：INTRODUCTION:In Argentina, hearing disability accounts for 18% of disabilities. Argentine Sign Language (ASL) is the communication system of choice used by deaf people (DP). An incorrect communication with physicians hampers the adequate provision of health care. DP require a professional ASL interpreter (PASLI) in the...

journal_title：Archivos argentinos de pediatria

authors： Cutri AM,Torres FA,Riquelme CC,Cabrera NB,Sandoval RR,Vesconi SM,Di Lalla S,Cordi L

更新日期：2018-10-01 00:00:00

abstract：:Tuberculosis is a common cause of morbimortality among children, especially in developing countries, where 95% of cases occur. Child tuberculosis is closely related to tuberculosis in the adult, since the diagnosis is an indicator of poor surveillance, treatment, and effort to eradicate it. Tuberculous lymphadenitis (...

journal_title：Archivos argentinos de pediatria

authors： Didier Cruz Anleu I,Velázquez Serratos JR,Alejandre García A

更新日期：2011-04-01 00:00:00