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Tegesé saka "galactosaemia" ing bausastra Basa Inggris

Bausastra
BAUSASTRA
section

PANGOCAP SAKA GALACTOSAEMIA ING BASA INGGRIS

galactosaemia  [ɡəˌlæktəˈsiːmɪə] play
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GOLONGAN PARAMASASTRA SAKA GALACTOSAEMIA

tembung aran
tembung sipat
tembung kriya
tembung katrangan
tembung ganti
preposition
panyambung
panemtu
seru

APA TEGESÉ GALACTOSAEMIA ING BASA INGGRIS?

Klik kanggo deleng deifinisi asli saka «galactosaemia» ing bausastra Basa Inggris.
Klik kanggo deleng pertalan otomatis saka definisi ing Basa Jawa.

Galactosemia

Galactosemia

Galactosemia iku kelainan métabolik genetika langka sing duweni kemampuan individu kanggo metabolisme gula galaktosa kanthi bener. Galactosemia dumadi saka modhut warisan autosomal sing menehi kurang ing enzim sing tanggung jawab kanggo galurosa galur degradasi. Friedrich Goppert, salah sawijining Dokter Jerman, sepisanan nyatake penyakit iki ing taun 1917, amarga penyebabe minangka cacat ing metabolisme galaktosa sing diidentifikasi dening grup sing dipimpin dening Herman Kalckar ing taun 1956. Kejadian iki kira-kira 1 kanggo 60.000 kelahiran kanggo wong-wong Eropa. Ing populasi liya, tingkat insiden beda. Galactosemia sepuluh kaping luwih umum ing populasi Irlandia. Galactosemia is a rare genetic metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly. Galactosemia follows an autosomal recessive mode of inheritance that confers a deficiency in an enzyme responsible for adequate galactose degradation. Friedrich Goppert, a German Physician, first described the disease in 1917, with its cause as a defect in galactose metabolism being identified by a group led by Herman Kalckar in 1956. Its incidence is about 1 per 60,000 births for people of European ancestry. In other populations the incidence rate differs. Galactosemia is ten times more common within the Irish Traveller population.

Definisi saka galactosaemia ing bausastra Basa Inggris

Definisi Galactosaemia ing kamus iku kelainan genetis sing bisa nyebabake kemampuan manungsa kanggo metabolisme galaktosa, sing bisa didelok dening anané galaktosa ing getih.

The definition of galactosaemia in the dictionary is a genetic disorder which affects a person's ability to metabolise galactose, identifiable by the presence of galactose in the blood.

Klik kanggo deleng deifinisi asli saka «galactosaemia» ing bausastra Basa Inggris.
Klik kanggo deleng pertalan otomatis saka definisi ing Basa Jawa.

TEMBUNG BASA INGGRIS KANG KALARAS PADHA KARO GALACTOSAEMIA


anoxemia
ˌænɒkˈsiːmɪə
glycaemia
ˌɡlaɪˈsiːmɪə
glycemia
ˌɡlaɪˈsiːmɪə
hypercalcaemia
ˌhaɪpəkælˈsiːmɪə
hypercalcemia
ˌhaɪpəkælˈsiːmɪə
hyperglycaemia
ˌhaɪpəɡlaɪˈsiːmɪə
hyperglycemia
ˌhaɪpəɡlaɪˈsiːmɪə
hyperuricemia
ˌhaɪpəˌjʊərɪˈsiːmɪə
hypocalcemia
ˌhaɪpəʊkælˈsiːmɪə
hypoglycaemia
ˌhaɪpəʊɡlaɪˈsiːmɪə
hypoglycemia
ˌhaɪpəʊɡlaɪˈsiːmɪə
hypomagnesaemia
ˌhaɪpəʊˌmæɡnəˈsiːmɪə
hypomagnesemia
ˌhaɪpəʊˌmæɡnəˈsiːmɪə
hypoxaemia
ˌhaɪpɒkˈsiːmɪə
hypoxemia
ˌhaɪpɒkˈsiːmɪə
septicaemia
ˌsɛptɪˈsiːmɪə
septicemia
ˌsɛptɪˈsiːmɪə
thalassaemia
ˌθæləˈsiːmɪə
thalassemia
tæləˈsiːmɪə
toxemia
tɒkˈsiːmɪə

TEMBUNG BASA INGGRIS KANG AWIT KAYA GALACTOSAEMIA

galactagogue
galactic
galactic circle
galactic equator
galactic halo
galactic plane
galactic poles
Galactico
galactometer
galactometry
galactophorous
galactopoiesis
galactopoietic
galactorrhoea
galactosamine
galactose
galactosemic
galactosidase
galactoside
galactosyl

TEMBUNG BASA INGGRIS KANG WUSANANÉ KAYA GALACTOSAEMIA

academia
anaemia
aplastic anaemia
bacteraemia
hyperaemia
hypercholesterolaemia
hyperlipidaemia
hypernatraemia
hyponatraemia
ischaemia
leukaemia
lymphoblastic leukaemia
megaloblastic anaemia
oligaemia
parasitaemia
pernicious anaemia
polycythaemia
pyaemia
sickle-cell anaemia
uraemia
viraemia

Dasanama lan kosok bali saka galactosaemia ing bausastra dasanama Basa Inggris

DASANAMA

Pertalan saka «galactosaemia» menyang 25 basa

PAMERTAL
online translator

PERTALAN SAKA GALACTOSAEMIA

Weruhi pertalan saka galactosaemia menyang 25 basa nganggo Basa Inggris pamertal multi basa kita.
pertalan saka galactosaemia saka Basa Inggris menyang basa liyané kang kasuguhaké ing perangan iki kajupuk saka pertalan statistik otomatis; ing ngendhi inti unit pertalan yaiku tembung «galactosaemia» ing Basa Inggris.

Pamertal Basa Inggris - Basa Cina

galactosaemia
1,325 yuta pamicara

Pamertal Basa Inggris - Basa Spanyol

galactosemia
570 yuta pamicara

Basa Inggris

galactosaemia
510 yuta pamicara

Pamertal Basa Inggris - Basa India

galactosaemia
380 yuta pamicara
ar

Pamertal Basa Inggris - Basa Arab

galactosaemia
280 yuta pamicara

Pamertal Basa Inggris - Basa Rusia

Галактоземия
278 yuta pamicara

Pamertal Basa Inggris - Basa Portugis

galactosemia
270 yuta pamicara

Pamertal Basa Inggris - Basa Bengali

galactosaemia
260 yuta pamicara

Pamertal Basa Inggris - Basa Prancis

galactosémie
220 yuta pamicara

Pamertal Basa Inggris - Basa Malaysia

Galactosaemia
190 yuta pamicara

Pamertal Basa Inggris - Basa Jerman

Galaktosämie
180 yuta pamicara

Pamertal Basa Inggris - Basa Jepang

galactosaemia
130 yuta pamicara

Pamertal Basa Inggris - Basa Korea

galactosaemia
85 yuta pamicara

Pamertal Basa Inggris - Basa Jawa

Galactosaemia
85 yuta pamicara
vi

Pamertal Basa Inggris - Basa Vietnam

galactosaemia
80 yuta pamicara

Pamertal Basa Inggris - Basa Tamil

galactosaemia
75 yuta pamicara

Pamertal Basa Inggris - Basa Marathi

गॅलेक्टोसिमीया
75 yuta pamicara

Pamertal Basa Inggris - Basa Turki

Galaktozemi
70 yuta pamicara

Pamertal Basa Inggris - Basa Italia

galattosemia
65 yuta pamicara

Pamertal Basa Inggris - Basa Polandia

galaktozemią
50 yuta pamicara

Pamertal Basa Inggris - Basa Ukrania

галактоземия
40 yuta pamicara

Pamertal Basa Inggris - Basa Romawi

galactozemie
30 yuta pamicara
el

Pamertal Basa Inggris - Basa Yunani

γαλακτοζαιμίας
15 yuta pamicara
af

Pamertal Basa Inggris - Basa Afrikaans

Galaktosemie
14 yuta pamicara
sv

Pamertal Basa Inggris - Basa Swedia

galaktosemi
10 yuta pamicara
no

Pamertal Basa Inggris - Basa Norwegia

galaktosemi
5 yuta pamicara

Trèn migunakaké galactosaemia

TRÈN

KEKAREPAN PANGGUNAN ARAN «GALACTOSAEMIA»

0
100%
ARANG KEREPÉ
Umum digunakaké
57
/100
Kart kang kapituduh ing dhuwur nuduhaké arang kerepé kagunané aran «galactosaemia» ing negara kang béda-béda.
Dhasar kekarepan panggolékan lan kagunaan kang umum saka galactosaemia
Daptar dhasar panggolékan kang dilakoni dening pangguna kanggo migunakaké Basa Inggris bausastra online kita lan gupita kang asring digunakaké nganggo tembung «galactosaemia».

ARANG KEREPÉ PANGGUNANÉ ARAN «GALACTOSAEMIA» SALAWASÉ IKI

Gambar awujudaké arang kerepé evolusi taunan panggunané saka tembung «galactosaemia» sasuwiné 500 taun. Panggunané andedhasar panalitén sapira asringé aran «galactosaemia» metu ing sumber kang kacé digital ing Basa Inggris antaraning taun 1500-an lan wektu iki.

Tuladha kang kagunakaké ing sastra Basa Inggris, pethikan lan warta babagangalactosaemia

TULADHA

BUKU BASA INGGRIS KAKAIT KARO «GALACTOSAEMIA»

Temukaké kagunané saka galactosaemia ing pilihan bibliografi iki. Buku kang kakait dening galactosaemia lan pethikan cekak kang padha kanggo nyediyakaké panggunané ing sastra Basa Inggris.
1
Babylove
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 ...
Robin Barker, 2007
2
Clinical Chemistry
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 ...
Puri, 2005
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 ...
Anthony P. Weetman, 1998
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 ...
Bruce E Murdoch, 2003

BABAGAN WARTA KANG NGLEBOKAKÉ ARAN «GALACTOSAEMIA»

Weruhi yèn pawarta nasional lan internasional wis ngomongaké lan kepriyé aran galactosaemia digunakaké ing babagan warta iki.
1
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»
2
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»
3
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»
4
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, Des 13»
5
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, Jul 13»
6
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»
7
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»
8
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»
9
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, Jan 13»
10
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, Jul 12»

KAITAN
« EDUCALINGO. Galactosaemia [online]. Kasedya <https://educalingo.com/jv/dic-en/galactosaemia>. Mei 2024 ».
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