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JIMD Reports - Volume 11

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Cover of 'JIMD Reports - Volume 11'

Table of Contents

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    Book Overview
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    Chapter 214 Enzyme Replacement Therapy in a Patient with Gaucher Disease Type III: A Paradigmatic Case Showing Severe Adverse Reactions Started a Long Time After the Beginning of Treatment
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    Chapter 215 Expanding the Spectrum of Methylmalonic Acid-Induced Pallidal Stroke: First Reported Case of Metabolic Globus Pallidus Stroke in Transcobalamin II Deficiency
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    Chapter 216 A Large Intragenic Deletion in the ACADM Gene Can Cause MCAD Deficiency but is not Detected on Routine Sequencing
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    Chapter 217 Infantile Hypophosphatasia Secondary to a Novel Compound Heterozygous Mutation Presenting with Pyridoxine-Responsive Seizures
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    Chapter 218 Liver Transplantation Prevents Progressive Neurological Impairment in Argininemia
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    Chapter 219 Motor and Speech Disorders in Classic Galactosemia.
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    Chapter 220 Defect of Cobalamin Intracellular Metabolism Presenting as Diabetic Ketoacidosis: A Rare Manifestation.
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    Chapter 221 Cerebral Magnetic Resonance Spectroscopy Demonstrates Long-Term Effect of Bone Marrow Transplantation in α-Mannosidosis
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    Chapter 222 Early Cardiac Changes in Children with Anderson–Fabry Disease
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    Chapter 223 Development of a Scoring System to Evaluate the Severity of Craniocervical Spinal Cord Compression in Patients with Mucopolysaccharidosis IVA (Morquio A Syndrome)
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    Chapter 224 Outcome of Perinatal Hypophosphatasia in Manitoba Mennonites: A Retrospective Cohort Analysis
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    Chapter 225 Novel Deletion Mutation Identified in a Patient with Late-Onset Combined Methylmalonic Acidemia and Homocystinuria, cblC Type.
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    Chapter 226 Substrate Reduction Therapy in Four Patients with Milder CLN1 Mutations and Juvenile-Onset Batten Disease Using Cysteamine Bitartrate.
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    Chapter 227 A Clinically Severe Variant of β-Mannosidosis, Presenting with Neonatal Onset Epilepsy with Subsequent Evolution of Hydrocephalus
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    Chapter 228 A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth Syndrome
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    Chapter 229 Selective Screening for Lysosomal Storage Diseases with Dried Blood Spots Collected on Filter Paper in 4,700 High-Risk Colombian Subjects
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    Chapter 230 Mitochondrial Infantile Liver Disease due to TRMU Gene Mutations: Three New Cases
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    Chapter 231 Spondyloepiphyseal Dysplasias and Bilateral Legg-Calvé-Perthes Disease: Diagnostic Considerations for Mucopolysaccharidoses
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    Chapter 232 Severe Neonatal Metabolic Decompensation in Methylmalonic Acidemia Caused by CblD Defect.
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    Chapter 233 Socio-emotional Problems in Children with CDG
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    Chapter 235 Metabolic Profiling of Total Homocysteine and Related Compounds in Hyperhomocysteinemia: Utility and Limitations in Diagnosing the Cause of Puzzling Thrombophilia in a Family
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    Chapter 236 Fatty Acid Oxidation Disorders in a Chinese Population in Taiwan
Attention for Chapter 220: Defect of Cobalamin Intracellular Metabolism Presenting as Diabetic Ketoacidosis: A Rare Manifestation.
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Chapter title
Defect of Cobalamin Intracellular Metabolism Presenting as Diabetic Ketoacidosis: A Rare Manifestation.
Chapter number 220
Book title
JIMD Reports - Volume 11
Published in
JIMD Reports, April 2013
DOI 10.1007/8904_2013_220
Pubmed ID
Book ISBNs
978-3-64-237327-5, 978-3-64-237328-2
Authors

Sheetal Sharda, Suresh Kumar Angurana, Mandeep Walia, Savita Attri

Editors

Johannes Zschocke, K Michael Gibson, Garry Brown, Eva Morava, Verena Peters

Abstract

Hypoglycemia is the usual feature of commonly occurring organic acidemias. Organic acidemias manifesting as hyperglycemia or diabetic ketoacidosis are rare and only a few cases have been reported. We report a 13-month-old boy who presented with vomiting, dehydration, coma, hyperglycemia, high anion gap metabolic acidosis and ketosis, mimicking diabetic ketoacidosis (DKA). Treatment with parenteral fluid, electrolytes, and insulin infusion resulted in an improvement in hyperglycemia, but persistence of metabolic acidosis and lack of improvement of neurologic status led us to suspect an organic acidemia. Urinary organic acid analysis revealed increased methylmalonic acid levels. In addition, hyperhomocysteinemia and homocystinuria were also noted in presence of normal vitamin B12 levels. This confirmed the diagnosis of cobalamin metabolism defect leading to combined methylmalonic aciduria and homocystinuria. There was some improvement in neurologic status and metabolic parameters after treatment with low-protein diet, vitamin B12, folic acid, and L-carnitine, but he ultimately succumbed to polymicrobial nosocomial sepsis. The entire MMACHC gene of the patient was sequenced and no mutations were identified. This is probably the first case report of cobalamin intracellular metabolism defect (CblC/CblD/CblF/CblJ or ABCD4) presenting as diabetic ketoacidosis.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 19 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 19 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 4 21%
Student > Ph. D. Student 3 16%
Researcher 3 16%
Student > Master 3 16%
Student > Doctoral Student 1 5%
Other 3 16%
Unknown 2 11%
Readers by discipline Count As %
Medicine and Dentistry 6 32%
Biochemistry, Genetics and Molecular Biology 3 16%
Agricultural and Biological Sciences 3 16%
Nursing and Health Professions 2 11%
Arts and Humanities 1 5%
Other 3 16%
Unknown 1 5%
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 13 September 2023.
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#20,242,136
of 22,769,322 outputs
Outputs from JIMD Reports
#482
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#174,549
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Outputs of similar age from JIMD Reports
#8
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