Journals / Türk Göğüs Kalp Damar Cerrahisi Dergisi / 2015 / Cilt: 23 - Sayı: 3

Apical hypertrophic cardiomyopathy in childhood: a very rare variant

Çocuklukta apikal hipertrofik kardiyomiyopati: çok nadir bir değişken

Pages
549–551
Publication Date
2022-09-02
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this article, we describe the clinical presentation of a seven-year-old girl who was asymptomatic, presented for cardiac evaluation and was detected to have an apical variant of hypertrophic cardiomyopathy.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Apical hypertrophic cardiomyopathy is a rare form of hypertrophic cardiomyopathy which classically involves the apex of the left ventricle.
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Key Findings & Data:Apical hypertrophic cardiomyopathy can be an incidental finding, or patients may present with chest pain, palpitations, dyspnea, and syncope.
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Conclusion & Impact:In this article, we describe the clinical presentation of a seven-year-old girl who was asymptomatic, presented for cardiac evaluation and was detected to have an apical variant of hypertrophic cardiomyopathy.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Apical hypertrophic cardiomyopathy is a rare form of hypertrophic cardiomyopathy which classically involves the apex of the left ventricle. Apical hypertrophic cardiomyopathy can be an incidental finding, or patients may present with chest pain, palpitations, dyspnea, and syncope. In this article, we describe the clinical presentation of a seven-year-old girl who was asymptomatic, presented for cardiac evaluation and was detected to have an apical variant of hypertrophic cardiomyopathy.

Özet

Apikal hipertrofik kardiyomiyopati klasik olarak sol ventrikülün apeksini tutan nadir bir hipertrofik kardiyomiyopati kardiyomiyopati rastlantısal bir bulgu olabilir ya da hastalar göğüs ağrısı, çarpıntı, dispne ve senkop ile başvurabilir. Bu yazıda asemptomatik olan, kardiyak değerlendirme için başvuran ve hipertrofik kardiyomiyopatinin apikal bir değişkeni olduğu tespit edilen yedi yaşında bir kızın klinik görünümü tanımlandı.

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Cite This Article

ERTUĞRUL, İ., KAYALI, Ş., YOLDAŞ, T., KARADEMİR, S., DOĞAN, V., ÖRÜN, U. A. (2022). Apical hypertrophic cardiomyopathy in childhood: a very rare variant. Türk Göğüs Kalp Damar Cerrahisi Dergisi, Cilt: 23 - Sayı: 3, 549–551. https://ajindex.com/articles/424223

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References (8)

  1. Sakamoto T, Tei C, Murayama M, Ichiyasu H, Hada Y. Giant T wave inversion as a manifestation of asymmetrical apical hypertrophy (AAH) of the left ventricle. Echocardiographic and ultrasono-cardiotomographic study. Jpn Heart J 1976;17:611-29
  2. Miyamoto T, Horigome H, Kawano S, Sumazaki R. Apical hypertrophic cardiomyopathy in childhood: a long-term follow-up report of two cases. Pediatr Cardiol 2009;30:343-6
  3. Kitaoka H, Doi Y, Casey SA, Hitomi N, Furuno T, Maron BJ. Comparison of prevalence of apical hypertrophic cardiomyopathy in Japan and the United States. Am J Cardiol 2003;92:1183-6
  4. Arad M, Penas-Lado M, Monserrat L, Maron BJ, Sherrid M, Ho CY, et al. Gene mutations in apical hypertrophic cardiomyopathy. Circulation 2005;112:2805-11
  5. Maron BJ, McKenna WJ, Danielson GK, Kappenberger LJ, Kuhn HJ, Seidman CE, et al. American College of Cardiology/European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the European Society of Cardiology Committee for Practice Guidelines. Eur Heart J 2003;24:1965-91
  6. McKenna WJ, Spirito P, Desnos M, Dubourg O, Komajda M. Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families. Heart 1997;77:130-2
  7. Kubo T, Kitaoka H, Okawa M, Hirota T, Hoshikawa E, Hayato K, et al. Clinical profiles of hypertrophic cardiomyopathy with apical phenotype--comparison of pure-apical form and distal-dominant form. Circ J 2009;73:2330-6
  8. Eriksson MJ, Sonnenberg B, Woo A, Rakowski P, Parker TG, Wigle ED, et al. Long-term outcome in patients with apical hypertrophic cardiomyopathy. J Am Coll Cardiol 2002;39:638-45.