Hearing Loss in Mucopolysaccharidosis

Hearing Loss in Mucopolysaccharidosis

Introduction Mucopolysaccharidosis (MPS) is a set of rare diseases caused by deficiency of lysosomal enzymes that lead to the accumulation of glycosaminoglycans (GAG) in tissues and organs, which, in turn, is responsible for the multisystemic clinical, chronic, and progressive symptoms. O...

Full description

Bibliographic Details
Main Authors:	Cibele Gomes Bicalho, Emília Katiane Embiruçu de Araújo Leão, Álvaro Muiños de Andrade, Angelina Xavier Acosta
Format:	Article
Language:	English
Published:	Thieme Revinter Publicações Ltda. 2021-07-01
Series:	International Archives of Otorhinolaryngology
Subjects:	mucopolysaccharidosis otorhinolaryngology metabolism inborn errors of metabolism hearing loss
Online Access:	http://www.thieme-connect.de/DOI/DOI?10.1055/s-0040-1712107

Similar Items

Mucopolysaccharidosis type VI: case report with first neonatal presentation with ascites fetalis and rapidly progressive cardiac manifestation
by: Rachel Sayuri Honjo, et al.
Published: (2020-02-01)

Audiologic Evaluation of Patients with Mucopolysaccharidosis at a Pediatric Hospital
by: Gomes, Ariana Braga, et al.
Published: (2011-04-01)

Avaliação do comprometimento auditivo em pacientes com mucopolissacaridose
by: Bicalho, Cibele Gomes
Published: (2015)

Unveiling metabolic remodeling in mucopolysaccharidosis type III through integrative metabolomics and pathway analysis
by: Abdellah Tebani, et al.
Published: (2018-09-01)

Audiometric evaluation in individuals with mucopolysaccharidosis
by: Marcela Rosana Maia da Silveira, et al.
Published: (2018-12-01)

The importance of the otorhinolaryngologic evaluation in mucopolysaccharidosis patients
by: Bicalho, Cibele Gomes, et al.
Published: (2011-07-01)

Audiologic evaluations of children with mucopolysaccharidosis
by: Çağil Gökdoğan, et al.

Resultados del programa de pesquisaje neonatal de errores innatos del metabolismo en Las Tunas
by: Madelin Rodríguez Cruz, et al.
Published: (2016-04-01)

Inborn Errors of Fructose Metabolism. What Can We Learn from Them?
by: Christel Tran
Published: (2017-04-01)

Metabolic evaluation of children with global developmental delay
by: So-Hee Eun, et al.
Published: (2015-04-01)

Clinical and biochemical spectrum of metabolic cardiomyopathy in Egyptian children
by: Almenabawy, N.M, et al.
Published: (2022)

A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report
by: Caio Perez Gomes, et al.
Published: (2020-03-01)

Trends of congenital hypothyroidism and inborn errors of metabolism in Pakistan
by: Sumreena Mansoor
Published: (2020-11-01)

Inborn errors of metabolism: a clinical overview
by: Ana Maria Martins
Published: (1999-11-01)

Communication impairments in children with inborn errors of metabolism: A preliminary study
by: Shivani Tiwari, et al.
Published: (2017-01-01)

Towards an Algorithm-Based Tailored Treatment of Acute Neonatal Hyperammonemia
by: Sunny Eloot, et al.
Published: (2021-07-01)

Screening for Inborn Errors of Metabolism
by: F.A. Elshaari, et al.
Published: (2013-09-01)

Glutaric acidemia type I. Report of a case and literature review
by: Forero Sánchez, Edwin, et al.
Published: (2015-04-01)

A Rare Cause of Sudden Onset-Severe Metabolic Acidosis in Paediatric Surgical Patients- Organic Acidemia
by: Vipin Kumar Singh, et al.
Published: (2016-03-01)

MEDNIK syndrome: a new entry in the spectrum of inborn errors of copper metabolism
by: Gavino Faa, et al.
Published: (2020-05-01)

Does the patient have a leukodystrophy? Importance of clinical description, semiotics and neuroimaging in the diagnostic suspicion of a metabolicorigin leukodystrophy
by: Echeverri-Peña, Olga Yaneth, et al.
Published: (2017-04-01)

Sir Archibald Garrod
by: K Varadaraj Shenoy, et al.
Published: (2013-01-01)

Clinical characteristics of adult patients with inborn errors of metabolism in Spain: A review of 500 cases from university hospitals
by: J. Pérez-López, et al.
Published: (2017-03-01)

Fructose and Mannose in Inborn Errors of Metabolism and Cancer
by: Elizabeth L. Lieu, et al.
Published: (2021-07-01)

<i>Helicobacter pylori</i> Infection in Children with Phenylketonuria Does Not Depend on Metabolic Control and Is Not More Frequent Than in Healthy Subjects—A Cross-Sectional Study
by: Marek Walkowiak, et al.
Published: (2021-08-01)

Idiopathic Sudden Sensorineural Hearing Loss in Sweden : Diagnostic Protocol and Treatment in Relation to Outcome
by: Nosrati-Zarenoe, Ramesh
Published: (2009)

A 7-Year Report of Spectrum of Inborn Errors of Metabolism on Full-Term and Premature Infants in a Chinese Neonatal Intensive Care Unit
by: Wanqiao Zhang, et al.
Published: (2020-01-01)

Lesch-Nyhan Syndrome: a rare disorder of self-mutilating behavior
by: Mrinal Gupta, et al.
Published: (2014-01-01)

Screening for inborn errors of metabolism among newborns with metabolic disturbance and/or neurological manifestations without determined cause
by: Allan Chiaratti de Oliveira, et al.
Published: (2001-09-01)

Reducing posttraumatic stress in parents of patients with a rare inherited metabolic disorder using eye movement desensitization and reprocessing therapy: a case study
by: Thirsa Conijn, et al.
Published: (2021-03-01)

Infant mortality in Brazil attributable to inborn errors of metabolism associated with sudden death: a time-series study (2002–2014)
by: F. H. de Bitencourt, et al.
Published: (2019-02-01)

Metabolic Seizures
by: Mohammed Almannai, et al.
Published: (2021-07-01)

Propionic acidemia presenting as encephalopathy, hyper-ammonemia, recurrent pulmonary hemorrhage: A case report
by: Ramaning Loni, et al.
Published: (2020-01-01)

Selective screening for metabolic disorders in the Slovenian pediatric population
by: Repič-Lampret Barbka, et al.
Published: (2015-01-01)

Metabolic Evaluation of Epilepsy: A Diagnostic Algorithm With Focus on Treatable Conditions
by: Clara D. M. van Karnebeek, et al.
Published: (2018-12-01)

Newborn screening of inherited metabolic disorders by tandem mass spectrometry: past, present and future
by: G. Scaturro, et al.
Published: (2013-04-01)

APRESENTAÇÃO CLÍNICA INICIAL DOS CASOS DE ERROS INATOS DO METABOLISMO DE UM HOSPITAL PEDIÁTRICO DE REFERÊNCIA: AINDA UM DESAFIO DIAGNÓSTICO
by: Andressa Romão, et al.

Physiology, Psychoacoustics and Cognition in Normal and Impaired Hearing
Published: (2016)

Physiology, Psychoacoustics and Cognition in Normal and Impaired Hearing
Published: (2016)

Screening for aminoacidopathies using cost effective methods in symptomatic children: A cross sectional study
by: Nazmin Fatima, et al.
Published: (2021-02-01)

Cannot write session to /tmp/vufind_sessions/sess_86dufol6pkk9ajlrqb0nsij87j