0000000000850820

AUTHOR

Laura Cavallé-garrido

showing 3 related works from this author

Audiological Findings in Children With Mucopolysaccharidoses Type I–IV

2017

Abstract Objective The aim of our study is to reflect hearing impairment of 23 children diagnosed with mucopolysaccharidosis (MPS) type I, II, III and IV. Methods Retrospective study of the clinical, audiological and treatment (medical vs surgical) findings of 23 children diagnosed with MPS type I, II, III and IV followed at a Tertiary Referral Hospital between 1997 and 2015. Results Six cases of MPS I, 8 of MPS II, 4 of MPS III and 5 of MPS IV were reviewed. 71.2% of patients had secretory otitis media (SOM) and 54% of patients had some type of hearing loss (HL). The behaviour of hearing loss was variable in each of the subgroups of MPS, finding greater involvement and variability in types…

congenital hereditary and neonatal diseases and abnormalitiesPediatricsmedicine.medical_specialtyHearing lossbusiness.industryMucopolysaccharidosisnutritional and metabolic diseasesRetrospective cohort studyGeneral MedicineAudiologyTertiary referral hospitalmedicine.disease03 medical and health sciences0302 clinical medicineOtitisQuality of lifemedicinemedicine.symptomskin and connective tissue diseases030223 otorhinolaryngologybusiness030217 neurology & neurosurgeryActa Otorrinolaringologica (English Edition)
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Improving the Management of Patients with Hearing Loss by the Implementation of an NGS Panel in Clinical Practice

2020

A cohort of 128 patients from 118 families diagnosed with non-syndromic or syndromic hearing loss (HL) underwent an exhaustive clinical evaluation. Molecular analysis was performed using targeted next-generation sequencing (NGS) with a custom panel that included 59 genes associated with non-syndromic HL or syndromic HL. Variants were prioritized according to the minimum allele frequency and classified according to the American College of Medical Genetics and Genomics guidelines. Variant(s) responsible for the disease were detected in a 40% of families including autosomal recessive (AR), autosomal dominant (AD) and X-linked patterns of inheritance. We identified pathogenic or likely pathogen…

0301 basic medicineOncologyAdultMalemedicine.medical_specialtyAdolescentlcsh:QH426-470Hearing lossHearing Loss Sensorineuralclinical evaluationPopulationGenomicsDiseaseDeafnessArticle03 medical and health sciences0302 clinical medicineInternal medicinemedicineHumansgeneticsmolecular analysiseducationChildAllele frequencyGenetics (clinical)hearing losseducation.field_of_studybusiness.industryInfant NewbornHigh-Throughput Nucleotide SequencingInfantMiddle Agedmedicine.diseaselcsh:Genetics030104 developmental biologyChild PreschoolCohortMedical geneticsSensorineural hearing lossFemalenext-generation sequencingmedicine.symptombusiness030217 neurology & neurosurgeryGenes
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Hallazgos audiológicos en niños con mucopolisacaridosis tipos i - iv

2017

Resumen Objetivo Revision y descripcion de la afectacion otoaudiologica en el seguimiento de 23 ninos con diagnostico de mucopolisacaridosis (MPS) tipo  I , II , III y IV . Metodos Estudio retrospectivo de los hallazgos clinicos, audiologicos y tratamiento (medico y/o quirurgico) de 23 ninos con diagnostico de MPS tipo  I , II , III o IV en seguimiento en un hospital terciario entre 1997 y 2015. Resultados Seis casos de MPS  I , 8 de MPS  II , 4 de MPS  III y 5 de MPS  IV fueron revisados. Al inicio del seguimiento el 71,2% de los pacientes presentaban otitis media serosa (OMS) y el 54% de los casos presentaban algun tipo de hipoacusia. El comportamiento de la hipoacusia fue fluctuante en c…

0301 basic medicine03 medical and health sciences0302 clinical medicineOtorhinolaryngologybusiness.industryMedicine030105 genetics & heredity030223 otorhinolaryngologybusinessHumanitiesActa Otorrinolaringológica Española
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