Whole-exome sequencing reveals a novel mutation of MT-ND5 gene in a mitochondrial cardiomyopathy pedigree: Patients who show biventricular hypertrophy, hyperlactacidemia, pulmonary hypertension, and decreased exercise tolerance
Skeletal muscle biopsy histology showed predominantly raggedred fibers and few ragged blue fibers, which was consistent with mitochondrial myopathy.Conclusion: In the present study, we identified a novel mutation of MT-ND5, c.1315A>G (p.Thr439Ala), in a family pedigree using WES. (Anatol JCardiol 2019; 21: 18-24)
📌 3 Maddede Bu Makale
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Amaç & Hipotez:Objective: The aim of the present study was to determine whether pathogenic mutations were present in families with mitochondrial cardiomyopathy that presented during adolescence.Methods: The proband was a 21-year-old man who presented clinically with palpitations, chest tightness, pulmonary hypertension, and limitedexercise tolerance.
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Temel Bulgular & Veri:We determine whether pathogenicmutations were present by whole-exome sequencing (WES) in families.Results: Screening of the family using tandem mass spectrometry showed elevated lactic acid levels, glutaric aciduria, a mildly increasedglutarylcarnitine-to-octanoylcarnitine ratio, and normal bloodα-glucosidase, which was consistent with a respiratory chain complex 1 metabolicdisorder.
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Sonuç & Katkı:Skeletal muscle biopsy histology showed predominantly raggedred fibers and few ragged blue fibers, which was consistent with mitochondrial myopathy.Conclusion: In the present study, we identified a novel mutation of MT-ND5, c.1315A>G (p.Thr439Ala), in a family pedigree using WES. (Anatol JCardiol 2019; 21: 18-24)
🔬Tür:Araştırma Makalesi
📍Kapsam:2019 Verileri
⚙️Değişkenler:Alan Parametreleri
Özet
Objective: The aim of the present study was to determine whether pathogenic mutations were present in families with mitochondrial cardiomyopathy that presented during adolescence.Methods: The proband was a 21-year-old man who presented clinically with palpitations, chest tightness, pulmonary hypertension, and limitedexercise tolerance. Cardiac magnetic resonance imaging studies showed biventricular cardiac hypertrophy. We determine whether pathogenicmutations were present by whole-exome sequencing (WES) in families.Results: Screening of the family using tandem mass spectrometry showed elevated lactic acid levels, glutaric aciduria, a mildly increasedglutarylcarnitine-to-octanoylcarnitine ratio, and normal bloodα-glucosidase, which was consistent with a respiratory chain complex 1 metabolicdisorder. We identified a novel mutation of MT-ND5, c.1315A>G (p.Thr439Ala). Skeletal muscle biopsy histology showed predominantly raggedred fibers and few ragged blue fibers, which was consistent with mitochondrial myopathy.Conclusion: In the present study, we identified a novel mutation of MT-ND5, c.1315A>G (p.Thr439Ala), in a family pedigree using WES. (Anatol JCardiol 2019; 21: 18-24)
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Bu Makaleye Atıf Yap
ZHO, N., TANG, L., JİANG, Y., QİN, S., CUİ, J., WANG, Y., ZHU, W., ZHAO, W., PAN, C., SHU, X. (2019). Whole-exome sequencing reveals a novel mutation of MT-ND5 gene in a mitochondrial cardiomyopathy pedigree: Patients who show biventricular hypertrophy, hyperlactacidemia, pulmonary hypertension, and decreased exercise tolerance. The Anatolian Journal of Cardiology, Cilt: 21 - Sayı: 1, 18–24. https://ajindex.com/articles/365276
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