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Results 1 - 10 of 67 for Death in infancy
  1. CLN10 disease 
    ... disease leads to severe signs and symptoms and death in infancy.In the later-onset cases of CLN10 disease, CTSD gene mutations likely result in the production of a cathepsin D enzyme whose function is greatly reduced but not ... This condition is inherited in an autosomal ...
    https://medlineplus.gov/genetics/condition/cln10-disease - Genetics
  2. Brugada syndrome 
    ... Signs and symptoms related to arrhythmias, including sudden death, can occur from early infancy to late adulthood. Sudden death typically occurs around ...
    https://medlineplus.gov/genetics/condition/brugada-syndrome - Genetics
  3. Generalized arterial calcification of infancy 
    ... with this condition often do not survive past infancy, with death typically caused by a heart attack or stroke. ...
    https://medlineplus.gov/...ralized-arterial-calcification-of-infancy - Genetics
  4. Carnitine palmitoyltransferase I deficiency 
    ... nervous system damage, liver failure, coma, and sudden death. These problems can begin any time between infancy to adulthood, though some individuals experience no health ...
    https://medlineplus.gov/...rnitine-palmitoyltransferase-i-deficiency - Genetics
  5. Critical congenital heart disease 
    ... untreated, CCHD can lead to shock, coma, and death. However, most people with CCHD now survive past infancy due to improvements in early detection, diagnosis, and ...
    https://medlineplus.gov/.../critical-congenital-heart-disease - Genetics
  6. Short QT syndrome 
    ... and fainting (syncope) to cardiac arrest and sudden death. These signs and symptoms can occur any time from early infancy to old age. This condition may explain some ...
    https://medlineplus.gov/genetics/condition/short-qt-syndrome - Genetics
  7. Mitochondrial trifunctional protein deficiency 
    ... serious heart problems, breathing difficulties, coma, and sudden death. Signs and symptoms of mitochondrial trifunctional protein deficiency that may begin after infancy include hypotonia, muscle pain, a breakdown of muscle ...
    https://medlineplus.gov/...hondrial-trifunctional-protein-deficiency - Genetics
  8. Aicardi-Goutières syndrome 
    ... neurological problems and the highest risk for early death. People with the later-onset form of Aicardi-Goutières syndrome typically have normal development in infancy. In these individuals, encephalopathy typically occurs after 1 ...
    https://medlineplus.gov/.../condition/aicardi-goutieres-syndrome - Genetics
  9. Glycogen storage disease type 0 
    ... and sudden death, particularly after physical activity. Sudden death from cardiac arrest can occur in childhood or adolescence in people with muscle GSD 0.Individuals with liver GSD 0 usually show signs and symptoms of the disorder in infancy. People with this disorder develop low blood sugar ( ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-0 - Genetics
  10. Leigh syndrome 
    ... movement abilities (psychomotor regression) and typically results in death ... are usually vomiting, diarrhea, and difficulty swallowing (dysphagia), ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
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