With interest we read the article by Marseglia et al. about a 6yo boy with nemaline myopathy (NM) but without evidence for previous cardiac disease who ex-perienced non-triggered asystole, underwent prolonged resuscitation, and died 1 week later from secondary cerebral hypoxia [1]. We have the following comments and concerns. Was the previous history positive for palpitations, collapse, syncope, exertional dyspnea, or leg edema? Cardiac involvement in NM has been previously re-ported and includes sino-atrial block [2], WPW-syndrome [2], atrial fibrillation [3], bundle branch block [4], left anterior hemiblock [4], hypertrophic cardiomy-opathy [5], outflow tract obstruction [6], dilative car-diomyopathy [5], pulmonary hypertension [4], hear
The case of a neonate with a rapidly fatal course of nemaline myopathy is reported. Neonatal history...
Nemaline myopathy is a rare congenital disease that generally occurs in childhood. We report a case...
Cardiac involvement has not been a reported feature of congenital fiber-type disproportion myopathy....
Background: Nemaline myopathy is a rare, non progressive congenital skeletal muscle disorder defined...
Introduction: hypertrophic cardiomiopathy is a genetic-based pathology, characterised by a relevant ...
Aborted sudden cardiac death (SCD) has not been reported as initial manifestation of cardiac involve...
Nemaline myopathy is a rare congenital myopathy that generally presents in childhood. We report a ca...
Nonketotic hyperglycinemia is an autosomal recessive disorder of glycine metabolism characterized by...
PURPOSE: Sudden unexpected death autopsy is sometimes non-conclusive both from a macroscopic and fr...
Most cases of sudden cardiac death in young athletes (,35 years) are caused by inherited cardiomyopa...
We read with great interest the paper by Guhamajum-dar and Agarwala1 about Sweet syndrome,2 cutis la...
Purpose: Sudden unexpected death autopsy is sometimes non-conclusive both from a macroscopic and fro...
on hypertrophic cardiomyopathy ever addressed the real Recently, a report by the international long ...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
The heart and lung are in continuous reciprocal interaction that creates a functional and anatomical...
The case of a neonate with a rapidly fatal course of nemaline myopathy is reported. Neonatal history...
Nemaline myopathy is a rare congenital disease that generally occurs in childhood. We report a case...
Cardiac involvement has not been a reported feature of congenital fiber-type disproportion myopathy....
Background: Nemaline myopathy is a rare, non progressive congenital skeletal muscle disorder defined...
Introduction: hypertrophic cardiomiopathy is a genetic-based pathology, characterised by a relevant ...
Aborted sudden cardiac death (SCD) has not been reported as initial manifestation of cardiac involve...
Nemaline myopathy is a rare congenital myopathy that generally presents in childhood. We report a ca...
Nonketotic hyperglycinemia is an autosomal recessive disorder of glycine metabolism characterized by...
PURPOSE: Sudden unexpected death autopsy is sometimes non-conclusive both from a macroscopic and fr...
Most cases of sudden cardiac death in young athletes (,35 years) are caused by inherited cardiomyopa...
We read with great interest the paper by Guhamajum-dar and Agarwala1 about Sweet syndrome,2 cutis la...
Purpose: Sudden unexpected death autopsy is sometimes non-conclusive both from a macroscopic and fro...
on hypertrophic cardiomyopathy ever addressed the real Recently, a report by the international long ...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
The heart and lung are in continuous reciprocal interaction that creates a functional and anatomical...
The case of a neonate with a rapidly fatal course of nemaline myopathy is reported. Neonatal history...
Nemaline myopathy is a rare congenital disease that generally occurs in childhood. We report a case...
Cardiac involvement has not been a reported feature of congenital fiber-type disproportion myopathy....