213 results match your criteria: "Hospital Infantil la Fe[Affiliation]"

Introduction: Autism spectrum disorders make up a group of neurodevelopmental disorders that globally affect different higher brain functions in the individual, such as intelligence, the capacity to use language and social interaction. Today, although there is still no curative treatment for autism, there are a number of non pharmacological interventions that can modify the poor prognosis that is generally associated to this type of disorders.

Aim: To briefly review the different approaches to the neuro rehabilitation of patients suffering from autism spectrum disorders, which are usually known as methods of intervention.

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For the last ten years many centres have adopted transanal pull-through (TP) as the first choice technique for the treatment of Hirschsprung's Disease (HD) affected children. We present our experience, based on the endorectal pull-through with autosuture, which has not been reported up to now. According to our HD management programme, TP with autosuture should be performed in rectosigmoid forms of HD which are easily handled with outpatient care.

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Introduction: Familial hypercholesterolemia (FH) is characterized by exposure to severely elevated LDL-cholesterol from birth, which produces lipid deposits, which can be measured by means of intima-media thickness (IMT).

Subjects And Methods: The IMT and concentrations of cholesterol and its fractions, triglycerides, alipoproteins Apo-A1, Apo-B and endothelial risk factors (homocysteine and high sensitivity protein C ) were determined in 89 patients (44 males) from 2 to 19 years (9.54+/-3.

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Introduction And Aim: Weekly home-based subcutaneous immunoglobulin (SCIg) therapy is an alternative to intravenous immunoglobulin (IVIg) in the treatment of patients with primary antibody deficiencies. The objective of this study was to investigate the efficacy, safety, related quality of life and cost effectiveness of SCIg in our area.

Materials And Methods: Observational and descriptive study including paediatric patients with common variable immunodeficiency (CVID) receiving SCIg in our hospital (November 2006 to April 2008).

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Article Synopsis
  • A European study was conducted on infants with neuroblastoma and MYCN gene amplification, enrolling patients diagnosed between 1999 and 2004, focusing on various stages of the disease.
  • Among the 46 infants enrolled, 35 were eligible; most had advanced metastatic disease, resulting in a two-year overall survival rate of 30% and a median survival of just 12 months.
  • The induction chemotherapy was well tolerated, but 30% of patients did not respond, highlighting the need for new treatment strategies and greater international cooperation for better outcomes.
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Obstructive uropathy in a HIV+ infant under indinavir treatment.

J Pediatr Urol

December 2007

Pediatric Urology Unit, Hospital Infantil La Fe, Avenida de Campanar 21, 46009 Valencia, Spain.

The case is presented of a 10-year-old HIV+ male with renoureteral pain, who developed an obstructive uropathy with renal function impairment and required endoscopic placement of a ureteral stent. Certain aspects of the epidemiology, clinical presentation, diagnosis, treatment and prevention are discussed.

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Introduction: Posttransplant lymphoproliferative disorder (PTLD) constitutes a heterogeneous group of diseases. We summarize the experience of our hospital, one of Spain's largest series of renal (294), liver (47) and allogeneic stem cell transplants (67), where four cases of PTLD have developed related to complex viral infections.

Methods: Case 1 was a 24-month-old boy diagnosed with acute lymphoblastic leukemia who underwent allogeneic stem-cell transplantation (SCT).

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Introduction: Primary cardiac tumours are very rare in the paediatric age, their incidence varies from 0.0017 % to 0.28 %.

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[Cow milk protein allergies: primary prevention. Nutritional aspects].

An Pediatr (Barc)

March 2008

Unidad de Nutrición y Metabolopatías, Hospital Infantil La Fe, Valencia, Spain.

In 2001 the Nutrition Committee of the Spanish Association of Pediatrics, published a position paper on "Recommendations on the use of formulae for the treatment and prevention of adverse reactions to cow milk proteins" (An Esp Pediatr. 2001;54:372-9). Since most of the recommendations given in this report still remain effective, the Nutrition Committee of the Spanish Association of Pediatrics reaffirms its support of the data expressed in it.

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Retrospective study of 124 patients (average age: 3.8 years) with midpenile hypospadias: 48.3% (60 children), distal penile: 45.

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Torsion of a cryptorchidid testicle presents a non-specific symptomatology. Clinical suspicion indicates surgical exploration, irrespective of Doppler ultrasound with its inherent false negative results. With regards to treatment, an orchiectomy is performed when the testis is necrotic.

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In this article, one of the novel mutations, c.208_209+ 8del10, was incorrectly given as c.69_70+8del10.

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The present article reviews the diagnostic criteria for pediatric obesity and its comorbidities. Treatment is also reviewed, including promotion of physical activity, and dietetic, pharmacologic and surgical treatment.

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Article Synopsis
  • The most common treatment for ADHD involves psychostimulants, but the presence of other disorders (comorbidities) requires a variety of therapeutic options to address the condition effectively.!* -
  • Understanding the various comorbidities is crucial for accurate diagnosis and timely intervention, which can improve treatment outcomes for ADHD patients.!* -
  • This paper provides an overview of the comorbid disorders related to ADHD and examines the pharmacological options available to mitigate their negative impacts.!*
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Accidental ingestion of foreign bodies is a common problem in children, but ingestion of magnets is rare. When multiple magnets are ingested, they may attract each other through the intestinal walls, causing pressure necrosis, perforation, fistula formation, or intestinal obstruction; as has been reported in 13 cases in the past 10 years. We report the fifth case in the literature of intestinal perforation and fistula caused by the ingestion of 2 small magnetic pieces of a toy by a 3-year-old boy.

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Aims: The aim of this study is to report on the neuropsychological aspects of teenage patients with attention deficit hyperactivity disorder (ADHD), namely disorders affecting attention, memory, the executive functions and language. We also discuss how to perform neuropsychological and functional evaluation of the systems involved in attention, by means of haemodynamic (functional magnetic resonance imaging) and neurophysiological (magnetoencephalography) techniques. The comorbidities that most frequently occur in teenage patients with ADHD are also described.

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Birth trauma and development of growing fracture after coronal suture disruption.

Childs Nerv Syst

March 2007

Department of Pediatric Neurosurgery, Hospital Infantil La Fe, Avda. Campanar s/n., 46009 Valencia, Spain.

Introduction: A growing fracture is a rare complication of skull fractures characterized by progressive diastatic enlargement of the fracture line. Growing skull fractures related to birth trauma were only occasionally reported. As far as we know, only one previous case of a neonatal growing fracture secondary to coronal suture disruption has been reported.

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Classical homocystinuria is due to cystathionine beta-synthase (CBS) deficiency. More than 130 mutations, which differ in prevalence and severity, have been described at the CBS gene. Mutation p.

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Microcephaly-lymphoedema-chorioretinal dysplasia: three cases to delineate the facial phenotype and review of the literature.

Clin Dysmorphol

July 2005

Sheffield Children's Hospital, Sheffield, UK Northwick Park Hospital, London, UK Department of Paediatrics, Hospital de Txagorritxu, Vitoria, Spain Department of Paediatrics, Hospital Infantil La Fe, Valencia, Spain Nottingham City Hospital, Nottingham, UK.

Microcephaly-lymphoedema-chorioretinal dysplasia (MIM 152950) has been described as a distinct clinical entity. The mode of inheritance is uncertain, but male to male transmission has been observed supporting autosomal dominant inheritance. A characteristic facial phenotype has recently been suggested.

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[Left renal vein hypertension syndrome].

Nefrologia

January 2006

Servicio de Nefrología Pediátrica, Hospital Infantil La Fe, Valencia.

Introduction: [corrected] Left renal vein compression, causing retrograde hypertension, determines a syndrome characterized by the presence of hematuria, gonadal vein dilatation and varicocele. Being a rare cause of hematuria its aetiology is diverse but of precise characteristics. Diagnosis is not easy and treatment requires to rule out its precise aetiology and consider the intensity of the compression phenomenon because of interventionist attitudes have important implications and are not risk free.

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