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JIMD Reports, Volume 35

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Cover of 'JIMD Reports, Volume 35'

Table of Contents

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    Book Overview
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    Chapter 16 Cerebrotendinous Xanthomatosis Presenting with Infantile Spasms and Intellectual Disability
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    Chapter 17 Hyperammonemia as a Presenting Feature in Two Siblings with FBXL4 Variants
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    Chapter 18 Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children’s Hospital
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    Chapter 18 Erratum to: White Matter Microstructure and Subcortical Gray Matter Structure Volumes in Aspartylglucosaminuria; a 5-Year Follow-up Brain MRI Study of an Adolescent with Aspartylglucosaminuria and His Healthy Twin Brother
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    Chapter 19 Severe Respiratory Acidosis in Status Epilepticus as a Possible Etiology of Sudden Death in Lesch–Nyhan Disease: A Case Report and Review of the Literature
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    Chapter 20 Vitamin B12 Administration by Subcutaneous Catheter Device in a Cobalamin A (cblA) Patient
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    Chapter 21 Expansion of the Phenotypic Spectrum of Propionic Acidemia with Isolated Elevated Propionylcarnitine
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    Chapter 22 Development of a Tandem Mass Spectrometry Method for Rapid Measurement of Medium- and Very-Long-Chain Acyl-CoA Dehydrogenase Activity in Fibroblasts
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    Chapter 23 Previously Unreported Biallelic Mutation in DNAJC19: Are Sensorineural Hearing Loss and Basal Ganglia Lesions Additional Features of Dilated Cardiomyopathy and Ataxia (DCMA) Syndrome?
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    Chapter 24 Lysosomal Storage Disorders in Nonimmune Hydrops Fetalis (NIHF): An Indian Experience
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    Chapter 25 The Risk of Fatty Acid Oxidation Disorders and Organic Acidemias in Children with Normal Newborn Screening
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    Chapter 26 Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency
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    Chapter 27 Analysis of Melanin-like Pigment Synthesized from Homogentisic Acid, with or without Tyrosine, and Its Implications in Alkaptonuria
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    Chapter 28 Bone Health in Classic Galactosemia: Systematic Review and Meta-Analysis
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    Chapter 29 Atypical Presentation and Treatment Response in a Child with Familial Hypercholesterolemia Having a Novel LDLR Mutation
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    Chapter 31 Cognitive Development in a Young Child with Mucolipidosis Type IV: A Case Report
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    Chapter 36 White Matter Microstructure and Subcortical Gray Matter Structure Volumes in Aspartylglucosaminuria; a 5-Year Follow-up Brain MRI Study of an Adolescent with Aspartylglucosaminuria and His Healthy Twin Brother
Attention for Chapter 18: Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children’s Hospital
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Chapter title
Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children’s Hospital
Chapter number 18
Book title
JIMD Reports, Volume 35
Published in
JIMD Reports, November 2016
DOI 10.1007/8904_2016_18
Pubmed ID
Book ISBNs
978-3-66-255832-4, 978-3-66-255833-1
Authors

Martín-Begué, Nieves, Alarcón, Silvia, Wolley-Dod, Charlotte, Lara, Luis Enrique, Madrid, Álvaro, Cano, Paola, Del Toro, Mireia, Ariceta, Gema, Nieves Martín-Begué, Silvia Alarcón, Charlotte Wolley-Dod, Luis Enrique Lara, Álvaro Madrid, Paola Cano, Mireia del Toro, Gema Ariceta, del Toro, Mireia

Abstract

Cystinosis is a rare systemic lysosomal disease affecting mainly the kidney and eye. Ocular involvement in cystinosis is universal being the presence of cystine crystals in the cornea a diagnostic criterion and one of the earliest manifestations of the disease. Neuro-ophthalmologic manifestations are considered a rare and late complication in these patients. The aim of this article is to report the unexpectedly high incidence of intracranial hypertension in children with cystinosis at our centre. This study included eight children (0-16 years of age) with cystinosis seen at the paediatric ophthalmology department, Hospital Universitari Vall d'Hebron (Barcelona, Spain), a tertiary hospital, over the last 5 years. Three girls and five boys, mean age: 9.6 years (range: 5-14 years), were studied. During follow-up, 4 out of 8 developed papilledema and confirmed high cerebrospinal fluid (CSF) pressure. The only symptomatic child presented an Arnold-Chiari anomaly with enlarged ventricles, whereas the other three, all asymptomatic, were diagnosed by scheduled fundoscopy and had normal neuroimaging studies. All four patients had at least one known risk factor for developing intracranial hypertension: initiation of growth hormone therapy, tapering of corticosteroids, acute renal failure and Arnold-Chiari malformation. Two of them required a ventriculoperitoneal shunt. Our results show that intracranial hypertension can occur more frequently than expected in patients with cystinosis. Furthermore, visual prognosis depends on early diagnosis and prompt treatment. A multidisciplinary approach is necessary, and we recommend fundoscopic examinations in all paediatric patients with cystinosis whether or not they present symptoms.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 21 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 21 100%

Demographic breakdown

Readers by professional status Count As %
Other 7 33%
Researcher 3 14%
Student > Doctoral Student 2 10%
Student > Master 2 10%
Student > Bachelor 1 5%
Other 3 14%
Unknown 3 14%
Readers by discipline Count As %
Medicine and Dentistry 11 52%
Biochemistry, Genetics and Molecular Biology 2 10%
Social Sciences 2 10%
Neuroscience 1 5%
Unknown 5 24%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 22 November 2016.
All research outputs
#18,482,034
of 22,901,818 outputs
Outputs from JIMD Reports
#437
of 545 outputs
Outputs of similar age
#302,681
of 415,686 outputs
Outputs of similar age from JIMD Reports
#12
of 21 outputs
Altmetric has tracked 22,901,818 research outputs across all sources so far. This one is in the 11th percentile – i.e., 11% of other outputs scored the same or lower than it.
So far Altmetric has tracked 545 research outputs from this source. They receive a mean Attention Score of 2.8. This one is in the 11th percentile – i.e., 11% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 415,686 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 16th percentile – i.e., 16% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 21 others from the same source and published within six weeks on either side of this one. This one is in the 33rd percentile – i.e., 33% of its contemporaries scored the same or lower than it.