Skip to main content
Key Specialties
Cardiology Diabetology Endocrinology Gastroenterology Geriatrics and Gerontology Gynecology and Obstetrics Hematology Infectious Disease Internal Medicine Nephrology Neurology Oncology Pediatrics Respiratory Medicine Rheumatology Surgery
Congress Coverage
2024 ACC Congress 2023 ESMO Congress 2023 EASD Congress 2023 ERS Congress 2023 ESC Congress
Clinical Collections
Advances in Alzheimer’s

Keynote webinar | Spotlight on medication adherence

LIVE: Thursday 27th June 2024, 18:00-19:30 (CEST)
Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.
ADVANCED SEARCH
Log in
Top
Pediatric and Developmental Pathology
Published in: Pediatric and Developmental Pathology 6/2004

01-12-2004 | Symposium on Mitochondrial Disease

Neonatal Mitochondrial Cardiomyopathy

Author: G. P. Taylor

Published in: Pediatric and Developmental Pathology | Issue 6/2004

Login to get access

Excerpt

A woman, age 34 years and gravida 2, para 1, delivered a term male infant who weighed 3489 g after an uncomplicated pregnancy and labor. Apgar scores were 4, 9, and 10. Over the first 2 days, the infant had difficulty breastfeeding and showed some inspiratory stridor. Investigations showed a minor degree of laryngomalacia. The patient was discharged at age 10 days but was readmitted 3 days later because of increasing feeding difficulties and episodes of tachycardia and increased stridor. …
Literature
1.
Papdopoulou, LC, Sue, CM, Davidson, MM,  et al. 1999Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly geneNat Genet23333337
2.
Hart, Z, Chang, C-H 1988A newborn infant with respiratory distress and persistent stridulous breathingJ Pediatr113150155PubMed
3.
Zeviani, M, Dyke, DH, Servidei, S,  et al. 1986Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiencyArch Neurol4311981202PubMed
4.
Guenthard, J, Wyler, F, Fowler, B, Baumgartner, R 1995Cardiomyopathy in respiratory chain disordersArch Dis Child72223226PubMedCrossRef
5.
Anderson, PAW 1990Immature myocardiumMoller, JHNeal, WA eds. Fetal, Neonatal, Infant Cardiac DiseaseAppleton & LangeNorwalk CT3571
6.
Muller-Hocker, J 1989Cytochrome-c-oxidase deficient cardiomyocytes in the human heart - an age-related phenomenon. A histochemical and ultracytochemical studyAm J Pathol13411671173PubMed
7.
Sengers, RCA, Stadhouders, AM, Trijbels, JMF 1984Mitochondrial myopathies: clinical, morphological and biochemical aspectsEur J Pediatr141192207CrossRefPubMed
8.
DiMauro, S, Bonilla, E, Zeviani, M, Nakagawa, M, DeVivo, DC 1985Mitochondrial myopathiesAnn Neurol17521538PubMed
9.
Arbustini, E, Diegoli, M, Fasani, R,  et al. 1998Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathyAm J Pathol15315011510PubMed
10.
Pelosi, G, Agliati, G 1968The heart muscle in functional overload and hypoxia. A biochemical and ultrastructural studyLab Invest188693PubMed
11.
Brega, A, Narula, J, Arbustini, E 2001Functional, structural, and genetic mitochondrial abnormalities in myocardial diseasesJ Nucl Cardiol88997CrossRefPubMed
Metadata
Title
Neonatal Mitochondrial Cardiomyopathy
Author
G. P. Taylor
Publication date
01-12-2004
Publisher
Springer-Verlag
Published in
Pediatric and Developmental Pathology / Issue 6/2004
Print ISSN: 1093-5266
Electronic ISSN: 1615-5742
DOI
https://doi.org/10.1007/s10024-004-5050-5

Other articles of this Issue 6/2004

Pediatric and Developmental Pathology 6/2004 Go to the issue

Symposium on Mitochondrial Disease

Biochemical Approach to the Investigation of Pediatric Mitochondrial Disease

Original Articles

Expression of laminin and fibronectin in renal dysplasia

Case report

Extrapleural Benign Solitary Fibrous Tumor in the Shoulder of a 9-Year-Old Girl: Case Report and Review of the Literature

Perspectives in Pediatric Pathology

Viral Diseases of the Liver in Children: Diagnostic and Differential Diagnostic Considerations

Book Review

Clinical guide to inherited metabolic diseases

Original Article

Expression of Laminin and Fibronectin in Renal Dysplasia