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obstructive jaundice: palpable gall bladder w/ painless jaundice unlikely to be cholelithiasis Crichton-Browne sign: Sir James Crichton-Browne: neuropsychiatry 'general paresis' tremor at corners of mouth and of outer canthus Crowe sign: Frank W. Crowe: dermatology: neurofibromatosis type I: axillary freckling Cruveilhier–Baumgarten bruit
Many people never have symptoms. [1] Occasionally jaundice (a slight yellowish color of the skin or whites of the eyes) may occur. [1] Gilbert syndrome is due to a genetic variant in the UGT1A1 gene which results in decreased activity of the bilirubin uridine diphosphate glucuronosyltransferase enzyme.
Neonatal jaundice is a yellowish discoloration of the white part of the eyes and skin in a newborn baby due to high bilirubin levels. [1] Other symptoms may include excess sleepiness or poor feeding. [1] Complications may include seizures, cerebral palsy, or kernicterus. [1] In most of cases there is no specific underlying physiologic disorder. [2]
This is a list of people with Down syndrome, a condition also known as Down's syndrome or trisomy 21. Down syndrome is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. [1] It is typically associated with developmental delays, characteristic physical features, and mild to moderate intellectual disability ...
Reye syndrome occurs almost exclusively in children. While a few adult cases have been reported over the years, these cases do not typically show permanent neural or liver damage. Unlike in the United Kingdom, the surveillance for Reye syndrome in the United States is focused on people under 18 years of age. [citation needed]
Image credits: Bettmann / gettyimages #3 Connie Converse. Elizabeth Eaton Converse, most commonly known by her stage name Connie, is often hailed as one of the first modern singer-songwriters, and ...
Eddie Murphy, Martin Lawrence and more celebrities' children have embarked on romantic relationships over the years. News broke in July 2021 that the two comedians’ offspring were dating .
Most of the signs and symptoms of the Joubert syndrome appear very early in infancy with most children showing delays in gross motor milestones. [6] Although other signs and symptoms vary widely from individual to individual, they generally fall under the hallmark of cerebellum involvement or in this case, lack thereof.