Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 13 for "Cardiomyopathy," fatal
  1. Early-onset myopathy with fatal cardiomyopathy 
    Early-onset myopathy with fatal cardiomyopathy (EOMFC) is an inherited muscle disease that affects the skeletal muscles, which are used for movement, and the ...
    https://medlineplus.gov/...-onset-myopathy-with-fatal-cardiomyopathy - Genetics
  2. TTN gene 
    ... identified in people with early-onset myopathy with fatal cardiomyopathy (EOMFC), an inherited disease that affects both skeletal ... deletions cause a novel early-onset myopathy with fatal cardiomyopathy. Ann Neurol. 2007 Apr;61(4):340-51. ...
    https://medlineplus.gov/genetics/gene/ttn - Genetics
  3. ACAD9 deficiency 
    ... have an enlarged and weakened heart muscle (hypertrophic cardiomyopathy), which is typically fatal in infancy or childhood.Individuals with ACAD9 deficiency ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  4. Familial hypertrophic cardiomyopathy 
    ... A small number of affected individuals develop potentially fatal heart failure, which may require heart transplantation.Nonfamilial hypertrophic cardiomyopathy tends to be milder. This form typically begins ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  5. PRKAG2 gene 
    ... Increased alpha2 subunit-associated AMPK activity and PRKAG2 cardiomyopathy. ... MW. Fatal congenital heart glycogenosis caused by a recurrent activating ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  6. DOLK-congenital disorder of glycosylation 
    ... L, Mandel H, Wevers RA. Autosomal recessive dilated cardiomyopathy due to DOLK ... Severe, fatal multisystem manifestations in a patient with dolichol kinase- ...
    https://medlineplus.gov/...dolk-congenital-disorder-of-glycosylation - Genetics
  7. SUCLG1-related mitochondrial DNA depletion syndrome 
    ... abnormalities and thickening of the heart muscle (hypertrophic cardiomyopathy). In affected individuals, a substance called methylmalonic acid ... life. This form of the disorder is called fatal infantile lactic acidosis. Infants with fatal infantile lactic ...
    https://medlineplus.gov/...ated-mitochondrial-dna-depletion-syndrome - Genetics
  8. Glycogen storage disease type IV 
    ... needed for breathing. These babies often have dilated cardiomyopathy, which enlarges and weakens the heart (cardiac) muscle, ... childhood and is characterized by myopathy and dilated cardiomyopathy. The severity of this type of GSD IV ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-iv - Genetics
  9. Cytochrome c oxidase deficiency 
    ... that enlarges and weakens the heart muscle (hypertrophic cardiomyopathy). Another possible feature of this condition is an ... include loss of mental function, movement problems, hypertrophic cardiomyopathy, eating difficulties, and brain abnormalities. Cytochrome c oxidase ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
  10. RYR2 gene 
    ... cause a heart condition called arrhythmogenic right ventricular cardiomyopathy (ARVC). This condition causes part of the heart ... WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 NCBI Gene ClinVar Bhuiyan ZA, van den ...
    https://medlineplus.gov/genetics/gene/ryr2 - Genetics
previous · 1 · 2 · next