CONGENITAL MYOPATHY WITH COR PULMONALE: A CASE REPORT

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NOURI M.; RAJAEI SH.; SHAH MOHAMADI MOUSAVI A.

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Journal: Hormozgan Medical Journal Year:2004 | Volume:7 | Issue:4 Page(s): 223-226

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Title

CONGENITAL MYOPATHY WITH COR PULMONALE: A CASE REPORT

Author(s)

NOURI M. | RAJAEI SH. | SHAH MOHAMADI MOUSAVI A. | Issue Writer Certificate

Keywords

RESPIRATORY INSUFFICIENCYQ3

MUSCULAR DYSTROPHYQ4

CHILDQ2

Abstract

Introduction: Congenital myopathies are rare group of skeletal muscle disorders that are often hereditary. Infantile form of congenital myopathies usually have a rapidly progressive course leading to early death caused by respiratory complications, but when presenting in adults they are often asymptomatic. Case: We present a 71/2 years old girl referred to hospital with symptoms of weakness, cyanosis and dyspnea. Clinical and laboratory findings compatible with congenital myopathy, associated with cor pulmonale. Conclusion: Cardiac involvement in congenital myopathies are unusual, although cardiomyopathy and cor pulmonale have been reported.

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APA: Copy

NOURI, M., RAJAEI, SH., & SHAH MOHAMADI MOUSAVI, A.. (2004). CONGENITAL MYOPATHY WITH COR PULMONALE: A CASE REPORT . HORMOZGAN MEDICAL JOURNAL, 7(4), 223-226. SID. https://sid.ir/paper/60280/en

Vancouver: Copy

NOURI M., RAJAEI SH., SHAH MOHAMADI MOUSAVI A.. CONGENITAL MYOPATHY WITH COR PULMONALE: A CASE REPORT . HORMOZGAN MEDICAL JOURNAL[Internet]. 2004;7(4):223-226. Available from: https://sid.ir/paper/60280/en

IEEE: Copy

M. NOURI, SH. RAJAEI, and A. SHAH MOHAMADI MOUSAVI, “CONGENITAL MYOPATHY WITH COR PULMONALE: A CASE REPORT ,” HORMOZGAN MEDICAL JOURNAL, vol. 7, no. 4, pp. 223–226, 2004, [Online]. Available: https://sid.ir/paper/60280/en

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