CHE SIGNIFICA GALACTOSAEMIA IN INGLESE
galattosemia
La galattosemia è un disturbo metabolico genetico raro che influenza la capacità di un individuo di metabolizzare correttamente il galattosio di zucchero. La galattosemia segue una modalità autosomica recessiva di eredità che conferisce una carenza in un enzima responsabile dell'adeguata degradazione del galattosio. Friedrich Goppert, medico tedesco, ha descritto per la prima volta la malattia nel 1917, con la sua causa di difetto nel metabolismo del galattosio identificato da un gruppo guidato da Herman Kalckar nel 1956. La sua incidenza è di circa 1 per 60.000 nascite per persone di origine europea. In altre popolazioni il tasso di incidenza è diverso. La galattosemia è dieci volte più comune all'interno della popolazione dei viaggiatori irlandesi.
definizione di galactosaemia nel dizionario inglese
La definizione di galattosemia nel dizionario è una malattia genetica che colpisce la capacità di una persona di metabolizzare il galattosio, identificabile dalla presenza di galattosio nel sangue.
PAROLE IN INGLESE ASSOCIATE CON «GALACTOSAEMIA»
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10 LIBRI IN INGLESE ASSOCIATI CON «GALACTOSAEMIA»
Scopri l'uso di
galactosaemia nella seguente selezione bibliografica. Libri associati con
galactosaemia e piccoli estratti per contestualizzare il loro uso nella letteratura.
Galactosaemia is an extremely rare disorder caused by the accumulation in the
blood of one of the sugars (galactose) found in milk. Galactosaemia is one of the
few times breastfeeding is contraindicated. Babies with galactosaemia who ...
Three enzyme defects can cause galactosaemia, and exemplify the production of
a clinical syndrome due to the accumulation of a substrate of the missing enzyme
. In classic galactosaemia, the absence of the enzyme galactose 1-phosphate ...
William J. Marshall, William J. Marshall (Ph. D.), S. K. Bangert,
2008
3
Textbook Of Biochemistry
Galactosaemia Inborn errors due to deficiency of one of the enzymes of
galactose metabolism cause galactosaemia. The deficient enzyme may be
galactokinase, galactose 1-phosphate uridyl transferase, or rarely epimerase.
Deficiency of the ...
4
Inborn Metabolic Diseases: Diagnosis and Treatment
N Engl J Med 304:994-998 Waggoner DD, Buist NRM, Donnell GN (1990) Long-
term prognosis in galactosaemia: result of a survey of a 350 cases. J Inherit
Metab Dis 13:802-818 29. Gibson JB (1995) Gonadal function in galactosemics
and ...
John Fernandes, Jean-Marie Saudubray, Georges van den Berghe,
2006
5
Rapid Paediatrics and Child Health
Galactosaemia: Neonates present with prolonged jaundice (initially
unconjugated then conjugated), vomiting, hypoglycaemia and 2° convulsions.
Later present with cataracts, hepatosplenomegaly, stunted growth, ascites and
learning ...
Helen A. Brough, Ram Nataraja,
2011
6
Clinical Paediatric Dietetics
It is now known that significant amounts of endogenous galactose are formed in
patients with galactosaemia with release rates being several-fold higher in
infants than in adults [90]. It is estimated that adults produce approximately 13 mg
/kg ...
Vanessa Shaw, Margaret Lawson,
2013
7
Oxford Handbook of Children's and Young People's Nursing
Galactosaemia is an autosomal recessive inherited metabolic disorder of
carbohydrate metabolism, affecting metabolism of galactose (from the milk sugar
lactose). There are three inborn errors of galactose metabolism (see figure
opposite).
Edward Alan Glasper, Gillian McEwing, Jim Richardson,
2007
8
Oxford Textbook of Medicine
Definitive diagnosis by enzymatic assay of galactokinase in erythrocytes or
cultured fibroblasts differentiates the disorder from classic galactosaemia and
hypergalactosaemia due to vas— cular disease in the liver. Treatment with a
strict ...
9
Endocrine Autoimmunity and Associated Conditions
Metabolic: galactosaemia Galactosaemia is a rare inherited autosomal recessive
disorder due to a deficiency in the enzyme galactose-1 -phosphate uridyl
transferase (GALT) [59]. These patients develop hepatocellular, ocular, renal,
and ...
10
Acquired Neurological Speech/Language Disorders In Childhood
The toxic manifestations of galactosaemia are thought to result from the
accumulation of galactose-1-phosphate.The major symptoms of the condition
when the infant is exposed to galactose include cataract formation,
hepatosplenomegaly ...
10 NOTIZIE DOVE SI INCLUDE IL TERMINE «GALACTOSAEMIA»
Vedi di che si parla nei media nazionali e internazionali e come viene utilizzato il termine ino
galactosaemia nel contesto delle seguenti notizie.
Highbury girl nets two medals on top-level debut at Tennis …
The 14-year-old, who lives in Whistler Street and has a rare genetic disorder called galactosaemia, was elevated to the competition's first ... «Islington Gazette, feb 15»
Milk Intake and Risk of Mortality and Fractures
Portnoi PA, MacDonald A. Determination of the lactose and galactose content of cheese for use in the galactosaemia diet. J Hum Nutr Diet 2009;22:400-8. «Medscape, nov 14»
Hereditary metabolic disorders may be under-diagnosed
Among the most frequent HMDs in Ireland are Phenylketonuria (PKU), Galactosaemia (the latter two detected by the national newborn ... «Irish Medical Times, feb 14»
Win £100 Sainsbury's vouchers with your real Christmas food …
Please note: Just Milk Lactose Free* is not suitable for cows' milk allergy sufferers or those with Galactosaemia. *Less than 0.1% lactose. «goodtoknow, dic 13»
The woes of premature menopause
Women with a family history of premature menopause and enzyme defects (galactosaemia) are more likely to have an early onset of menopause. Chromosome ... «Wonder Woman, lug 13»
AKUH can now detect genetic disorders in newborns
For instance, a person suffering from galactosaemia has to avoid milk or any milk products all his life while a person with fructose intolerance ... «The Express Tribune, mar 13»
Cystic Fibrosis: 44 babies diagnosed since routine heel prick tests …
The test screens for phenylketonuria, homocystinuria, maple syrup urine disease, classical galactosaemia, congenital hypothyroidism and ... «Irish Independent, feb 13»
Calls for 'priceless resource' of heel prick test results to be saved
These are Phenylketonuria (PKU), Homocystinuria, Maple Syrup Urine Disease, Classical Galactosaemia, Congenital Hypothyroidism and, ... «Irish Times, feb 13»
Doctors slam HSE move to scrap gene data
The diseases screened for are: phenylketonuria, cystic fibrosis, congenital hypothyroidism, classical galactosaemia, homocystinuria, and maple ... «Irish Health, gen 13»
Non-invasive prenatal measurement of the fetal genome
... and immunological disorders such as phenylketonuria, galactosaemia, maple syrup urine disease, and severe combined immunodeficiency. «Nature.com, lug 12»