Create issue ticket

12 Possible Causes for ENZYMES,[email protected] 27

  • Polyostotic Fibrous Dysplasia

    The protein produced from the GNAS gene helps stimulate the activity of an enzyme called adenylate cyclase.[ghr.nlm.nih.gov] […] oligonucleotide hybridization 6 , PCR–restriction fragment length polymorphism 27 , PCR with peptide nucleic acid 28 , and PCR with pyrosequencing 19 .[nature.com] Blood count, electrocardiogram and serum liver enzymes were normal.[ijpeonline.biomedcentral.com]

  • Euryales Ferox

    Of these three antioxidant enzymes, glutathione peroxidase activity was most strongly induced.[nature.com] It has a prominent place in Indian dietary chart with medicinal values for respiratory, circulatory, digestive, renal, and reproductive diseases 19-27 .[niscair.res.in] They can be antibodies, enzymes, messenger, structural or storage and transport in nature.[healthdietmedicine.com]

  • Perforated Peptic Ulcer

    The acids and digestive enzymes present in stomach and intestine further damages the erosion.[tandurust.com] Digestive tract perforations at Point G Teaching Hospital in Bamako, Mali. Mali Med. 2012; 27 (1):19–22. [ PubMed ] 45. Furukawa A, Sakoda M, Yamasaki M, et al.[ncbi.nlm.nih.gov] Peptic ulcers sometimes penetrate completely through the stomach or intestinal wall, resulting in a hole -- or perforation -- and spillage of acid, digestive enzymes and partially[livestrong.com]

  • Gastric Fistula

    Serum angiotensin converting enzyme was within normal limits. Mantoux was 18 mm at 48 h.[wjgnet.com] China E-mail: [email protected] Received Date: October 19, 2015; Accepted Date: October 27, 2015; Published Date: November 08, 2015 Citation: Chowdhury ATMM, Feng DJ, Min[omicsonline.org] I had elevated liver enzymes prior to the procedure was was given the ok for surgery.[bariatric-surgery-source.com]

  • Congenital Disorder of Glycosylation Type 9

    If you have one of these disorders, you may not have enough enzymes to break down the carbohydrates. Or the enzymes may not work properly.[icdlist.com] , F) R141H/I153T NA 2 12 (22, F) R141H/I153T NA (8 m) 12 13 (27, M) R141H/P113L Digestive troubles (at birth) 14 14 (34, F) R141H/P113L Vomiting (at birth) 25 15 (19, F) R141H[ojrd.biomedcentral.com] Individuals with a CDG are missing one of the enzymes that is required for glycosylation. The type of CDG that a person has depends on which enzyme is missing.[rarediseases.info.nih.gov]

  • Congenital Disorder of Glycosylation Type 1o

    The RFT1 homolog (human homolog of the yeast Rft1 enzyme) is a flippase enzyme that is responsible for the translocation of the Man 5 -GlcNAc 2 -P-P-Dol intermediate from[themedicalbiochemistrypage.org] , F) R141H/I153T NA 2 12 (22, F) R141H/I153T NA (8 m) 12 13 (27, M) R141H/P113L Digestive troubles (at birth) 14 14 (34, F) R141H/P113L Vomiting (at birth) 25 15 (19, F) R141H[ojrd.biomedcentral.com] Congenital disorders of glycosylation (CDGs) are very rare genetic disorders that lack enzymes needed for glycosylation.[jaclinicalreports.springeropen.com]

  • Carbohydrate Deficient Glycoprotein Syndrome Type 1Y

    CDG is caused by a genetically inherited change or malfunction of one of these enzymes.[littleladybughugs.com] , F) R141H/I153T NA 2 12 (22, F) R141H/I153T NA (8 m) 12 13 (27, M) R141H/P113L Digestive troubles (at birth) 14 14 (34, F) R141H/P113L Vomiting (at birth) 25 15 (19, F) R141H[ojrd.biomedcentral.com] If you have one of these disorders, you may not have enough enzymes to break down the carbohydrates. Or the enzymes may not work properly.[icdlist.com]

  • Metastatic Liver Carcinoma

    Adverse events were generally limited to injection site reactions and photosensitivity and resolved without sequelae, with elevated liver enzymes observed during the first[ecancer.org] Seven guidelines were focused on a single treatment [13] , [16] , [19] , [26] , [27] , [50] , [52] .[journals.plos.org] Liver enzyme levels are often elevated when there is a problem. Blood or serum markers are substances in the blood that are linked to cancer.[healthline.com]

  • Congenital Disorder of Glycosylation Type 2L

    […] deficiency Glycogenosis due to glycogen branching enzyme deficiency, adult neuromuscular form Glycogenosis due to glycogen branching enzyme deficiency, childhood combined[orpha.net] , F) R141H/I153T NA 2 12 (22, F) R141H/I153T NA (8 m) 12 13 (27, M) R141H/P113L Digestive troubles (at birth) 14 14 (34, F) R141H/P113L Vomiting (at birth) 25 15 (19, F) R141H[ojrd.biomedcentral.com] CDG is caused by a genetically inherited change or malfunction of one of these enzymes.[lymphedemapeople.com]

  • Congenital Disorder of Glycosylation Type 2J

    […] deficiency Glycogenosis due to glycogen branching enzyme deficiency, adult neuromuscular form Glycogenosis due to glycogen branching enzyme deficiency, childhood combined[orpha.net] , F) R141H/I153T NA 2 12 (22, F) R141H/I153T NA (8 m) 12 13 (27, M) R141H/P113L Digestive troubles (at birth) 14 14 (34, F) R141H/P113L Vomiting (at birth) 25 15 (19, F) R141H[ojrd.biomedcentral.com] CDG is caused by a genetically inherited change or malfunction of one of these enzymes.[lymphedemapeople.com]

Further symptoms