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Nagel, B; Gruber-Sedlmayr, U; Uhrig, S; Stöllberger, C; Klopocki, E; Finsterer, J.
Left ventricular hypertrabeculation/noncompaction with epilepsy, other heart defects, minor facial anomalies and new copy number variants.
BMC Med Genet. 2012; 13(8):60-60 Doi: 10.1186/1471-2350-13-60 (- Case Report) [OPEN ACCESS]
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Leading authors Med Uni Graz
Nagel Bert Hermann Philipp
Co-authors Med Uni Graz
Gruber-Sedlmayr Ursula
Uhrig Sabine
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Abstract:
Background: Left ventricular hypertrabeculation/noncompaction (LVHT) is a cardiac abnormality of unknown etiology which has been described in children as well as in adults with and without chromosomal aberrations. LVHT has been reported in association with various cardiac and extracardiac abnormalities like epilepsy and facial dysmorphism. Case presentation: A unique combination of LVHT, atrial septal defect, pulmonary valve stenosis, aortic stenosis, epilepsy and minor facial anomalies is presented in a 5.5 years old girl. Microarray-based genomic hybridization (array-CGH) detected six previously not described copy number variants (CNVs) inherited from a clinically unaffected father and minimally affected mother, thus, most likely, not clinically significant but rare benign variants. Conclusions: Despite this complex phenotype de novo microdeletions or microduplications were not detected by array CGH. Further investigations, such as whole exome sequencing, could reveal point mutations and small indels as the possible cause.
Find related publications in this database (using NLM MeSH Indexing)
Aortic Valve Stenosis - diagnosis
Child, Preschool -
DNA Copy Number Variations -
Epilepsy - diagnosis
Face - abnormalities
Female -
Humans -
Isolated Noncompaction of the Ventricular Myocardium - diagnosis
Oligonucleotide Array Sequence Analysis -
Pulmonary Valve Stenosis - diagnosis

Find related publications in this database (Keywords)
Cardiomyopathy
Congenital heart disease
Neurology
Pediatrics
Array CGH
Hypertrabeculation
Seizures
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