Neuroradiologic Findings in Sengers Syndrome
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health
Reference15 articles.
1. Congenital cataract and mitochondrial myopathy of skeletal and heart muscle associated with lactic acidosis after exercise;Sengers;J Pediatr,1975
2. A retrospective study of patients with the hereditary syndrome of congenital cataract, mitochondrial myopathy of heart and skeletal muscle and lactic acidosis;van Ekeren;Eur J Pediatr,1993
3. Sengers disease: A rare association of hypertrophic cardiomyopathy and congenital cataracts;Mehnaz;Indian J Pediatr,2004
4. Adenine nucleotide translocator 1 deficiency associated with Sengers syndrome;Jordens;Ann Neurol,2002
5. Congenital hypertrophic cardiomyopathy, cataract, mitochondrial myopathy and defective oxidative phosphorylation in two siblings with Sengers-like syndrome;Morava;Eur J Pediatr,2004
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1. Mitochondrial phospholipid metabolism in health and disease;Journal of Cell Science;2023-09-01
2. A novel AGK splicing mutation in a patient with Sengers syndrome and left ventricular non-compaction cardiomyopathy;Pediatric Research;2023-02-09
3. Long term follow-up in two siblings with Sengers syndrome: Case report;Italian Journal of Pediatrics;2022-10-17
4. Sengers syndrome: a rare case of cardiomyopathy combined with congenital cataracts in an infant: post-mortem case report;Cardiovascular Pathology;2021-09
5. A case report of children of the same family presenting with congenital cataract- as part of a rare genetic disorder–Sengers Syndrome;Indian Journal of Ophthalmology;2020
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