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Quoted phrase not found in phrase index: "Sudden cardiac failure, infantile"
Page 1
Sudden Unexpected Death of Infantile Dilated Cardiomyopathy with JPH2 and PKD1 Gene Variants.
Miura A, Kondo H, Yamamoto T, Okumura Y, Nishio H. Miura A, et al. Int Heart J. 2020 Sep 29;61(5):1079-1083. doi: 10.1536/ihj.20-155. Epub 2020 Sep 2. Int Heart J. 2020. PMID: 32879264 Free article.
An echocardiogram showed left ventricular dilatation with thin walls, severe mitral valve regurgitation, and a reduced ejection fraction. She died of acute cardiac failure 3 hours after the sudden change. Postmortem analysis with light microscopy showed disar …
An echocardiogram showed left ventricular dilatation with thin walls, severe mitral valve regurgitation, and a reduced ejection fraction. Sh …
Sudden unexpected infantile death due to undiagnosed ventricular septal defect-associated heart failure with single coronary artery.
Kasuda S, Kudo R, Yuui K, Kondo T, Hatake K. Kasuda S, et al. Forensic Sci Med Pathol. 2019 Jun;15(2):300-303. doi: 10.1007/s12024-018-0066-8. Epub 2018 Dec 15. Forensic Sci Med Pathol. 2019. PMID: 30554350
Ventricular septal defect (VSD) generally has a good prognosis unless complicated by heart failure (HF). We report a case of sudden infant death because of clinically undiagnosed VSD in a seemingly healthy 16-day-old boy. Although a cardiac murm …
Ventricular septal defect (VSD) generally has a good prognosis unless complicated by heart failure (HF). We report a ca …
Idiopathic infantile arterial calcification: the spectrum of clinical presentations.
Chong CR, Hutchins GM. Chong CR, et al. Pediatr Dev Pathol. 2008 Sep-Oct;11(5):405-15. doi: 10.2350/07-06-0297.1. Epub 2007 Aug 23. Pediatr Dev Pathol. 2008. PMID: 17990935 Review.
We report the case of a 32-week-old infant with hydrops fetalis and heart failure who died at 4 days of age. At autopsy the infant was found to have cardiomegaly, myocardial infarctions and multifocal calcifications of the aorta and arteries in the lungs, heart …
We report the case of a 32-week-old infant with hydrops fetalis and heart failure who died at 4 days of age. At autopsy the in …
Kawasaki disease. Relationship with infantile periarteritis nodosa.
Tanaka N, Sekimoto K, Naoe S. Tanaka N, et al. Arch Pathol Lab Med. 1976 Feb;100(2):81-6. Arch Pathol Lab Med. 1976. PMID: 3150
Until 1972, Kawasaki disease, or acute febrile infantile mucocutaneous lymph node syndrome (MCLS), was considered in Japan to be a nonfatal disease with a favorable prognosis. ...Such vascular pathological findings may in fact represent the same entity as infanti …
Until 1972, Kawasaki disease, or acute febrile infantile mucocutaneous lymph node syndrome (MCLS), was considered in Japan to be a no …
Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish.
Zahka K, Kalidas K, Simpson MA, Cross H, Keller BB, Galambos C, Gurtz K, Patton MA, Crosby AH. Zahka K, et al. Heart. 2008 Oct;94(10):1326-30. doi: 10.1136/hrt.2007.127241. Epub 2008 May 8. Heart. 2008. PMID: 18467358
BACKGROUND: Familial hypertrophic cardiomyopathy (HCM) is a leading cause of sudden cardiac death among young and apparently healthy people. Autosomal dominant mutations within genes encoding sarcomeric proteins have been identified. An autosomal recessive form of H …
BACKGROUND: Familial hypertrophic cardiomyopathy (HCM) is a leading cause of sudden cardiac death among young and apparently h …
Hypoxic-ischaemic encephalopathy after near miss sudden infant death syndrome.
Constantinou JE, Gillis J, Ouvrier RA, Rahilly PM. Constantinou JE, et al. Arch Dis Child. 1989 May;64(5):703-8. doi: 10.1136/adc.64.5.703. Arch Dis Child. 1989. PMID: 2730124 Free PMC article.
Between 1982 and 1985, 14 infants aged 3-26 weeks presented with severe hypoxic episodes as a result of the 'near miss' sudden infant death syndrome (SIDS). They all had metabolic acidosis, cardiovascular instability, acute renal failure, ischaemic colitis, or acute …
Between 1982 and 1985, 14 infants aged 3-26 weeks presented with severe hypoxic episodes as a result of the 'near miss' sudden infant …
A case of sporadic infantile histiocytoid cardiomyopathy caused by the A8344G (MERRF) mitochondrial DNA mutation.
Vallance HD, Jeven G, Wallace DC, Brown MD. Vallance HD, et al. Pediatr Cardiol. 2004 Sep-Oct;25(5):538-40. doi: 10.1007/s00246-003-0446-y. Epub 2004 May 28. Pediatr Cardiol. 2004. PMID: 15164143
We describe a sporadic case of an infant with the A8344G mtDNA mutation who presented with failure to thrive and sudden unexpected death at 11 months of age. ...Both complexes I and IV of the respiratory chain were reduced in cardiac muscle. The A8344G mtDNA …
We describe a sporadic case of an infant with the A8344G mtDNA mutation who presented with failure to thrive and sudden unexpe …
Enzyme replacement therapy for infantile Pompe disease during the critical period and identification of a novel mutation.
But WM, Lee SH, Chan AO, Lau GT. But WM, et al. Hong Kong Med J. 2009 Dec;15(6):474-7. Hong Kong Med J. 2009. PMID: 19966354 Free article.
Pompe disease (acid maltase deficiency, glycogen storage disease type II) is a rare progressive autosomal recessive disorder caused by a deficiency of lysosomal hydrolase acid alpha-glucosidase. Historically, infantile-onset Pompe disease presents with cardiomegaly, hepato …
Pompe disease (acid maltase deficiency, glycogen storage disease type II) is a rare progressive autosomal recessive disorder caused by a def …