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Death in infancy
- ... 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 ... CATD_HUMAN cathepsin ...
- ... 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 ...
- ... lead to a severe loss of fluids and death in early infancy. Like the mutations that cause keratoderma with woolly ...
- ... lead to a severe loss of fluids and death in early infancy. The mutation found to cause LCEB, written as ...
- ... Signs and symptoms related to arrhythmias, including sudden death, can occur from early infancy to late adulthood. Sudden death typically occurs around ...
- ... with this condition often do not survive past infancy, with death typically caused by a heart attack or stroke. ...
- ... have died suddenly with no known cause in infancy (sudden infant death syndrome) or early adulthood (sudden unexplained nocturnal death). ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
