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"Sudden infant death with dysgenesis of the testes syndrome is a rare condition in the first year of life; its key features include abnormalities of the reproductive system in males, feeding difficulties, and breathing difficulties. Infants with SIDDT who are genetically male, with one X chromosome and one Y chromosome in each cell, have underdeveloped or abnormal testes. SIDDT has been linked to abnormal brain development, particularly the brainstem, which is the portion of the brain that is connected to the spinal cord. Affected infants also have unusual cry that has been traced to abnormal nerve connections between the brain and the voicebox, which is likely due to abnormal brain-to-voice ratios. "When infants' respiratory and heartbeats stop beating, the brainstem abnormalities lead to death in the first year of life"; affected infants' first year of life.
"Short QT syndrome is a condition that can cause a change in the heart's normal rhythm". The heart muscle takes less time than normal to recover between beats in people with this disorder. Short QT" stands for a specific pattern of heart activity that can be determined by an electrocardiogram, which is a test used to determine heart electrical activity. However, some people with short QT syndrome have no health issues attributed to the condition.
"Insulin regulates the amount of sugar that moves from the blood into cells for conversion to electricity conversion from blood to electricity. " Individuals with 3-hydroxyacyl-CoA deficiency are also vulnerable to ailments such as seizures, life-threatening heart and breathing difficulties, coma, and sudden death. This illness can cause sudden infant death syndrome (SIB), which is defined as unexplained death in infants younger than 1 year. Deficiency problems related to 3-hydroxyacyl-CoA deficiency can be triggered by fasting or infectious infections. This disorder is sometimes mistaken for Reye syndrome, a severe condition that can occur in children if they do not appear to be recovering from viral infections such as chicken pox or flu. The use of aspirin is attributed to the majority of cases of Reye syndrome in these viral infections.
"Hereditary hyperekplexia is a condition in which infants have increased muscle tone and an exaggerated startle reaction to unexpected stimuli, especially loud noises. " Infants with hereditary hyperekplexia have hypertonia at any time, except when they are sleeping. Muscle twitches when falling asleep and movements of the arms or legs when asleep are both typical signs and symptoms of hereditary hyperekplexia. Infants with hereditary hyperekplexia have recurrent seizures. By the time 1, the signs and symptoms of hereditary hyperekplexia have generally diminished. However, elderly people with hereditary hyperekplexia may still startle easily and have periods of rigidity, which can lead them to fall down. People with epilepsy with hereditary hyperekplexia have epilepsy and epilepsy have epilepsy-related epilepsy throughout their lives. "Understanded death in infants younger than one year can be explained by hereditary hyperekplexia. ".
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