Create issue ticket

1,750 Possible Causes for ABNORMAL, CIRRHOSIS,, DEPOSITION, FAMILIAL,, GLYCOGEN, OF, WITH

  • Alkaptonuria

    Pompe disease is characterised by deficiency of acid α-glucosidase that results in abnormal glycogen deposition in the muscles.[ncbi.nlm.nih.gov] […] findings of ochronotic arthropathy in whom alkaptonuria disappeared and the progressive course of the disease stopped after liver transplantation for hepatitis B-related cirrhosis[ncbi.nlm.nih.gov] Deposition was noted in the apical region of the cells. A lobar duct presented a large calculus with unusual deposits possibly associated with calcium salts.[ncbi.nlm.nih.gov] Our findings document a reversal of bone abnormalities and clinical symptoms in a case of alkaptonuria. The results should be confirmed in a larger study.[ncbi.nlm.nih.gov] We present 9 cases of alkaptonuria (two males and seven females) in one Jordanian family.[ncbi.nlm.nih.gov] Orchronotic arthropathy: disappearance of alkaptonuria and liver transplant for hepatitis B related cirrhosis.[wikilectures.eu] We also demonstrate that the abnormal spectra from ochronotic cartilage fit with the abnormality in the structure of collagen fibres at the ultrastructural level, whereby[ncbi.nlm.nih.gov]

    Missing: OF WITH
  • Glucagon

    G Proteins Transmit the Signal for the Initiation of Glycogen Breakdown Several hormones greatly affect glycogen metabolism.[ncbi.nlm.nih.gov] cirrhosis (scarring of the liver and poor liver function) Low blood sugar ( hypoglycemia ) Multiple endocrine neoplasia type I (disease in which one or more of the endocrine[medlineplus.gov] Two white women aged 49 and 60 years manifested marked central body fat deposition with severe lipoatrophy of their limbs and buttocks and pronounced acanthosis nigricans.[ncbi.nlm.nih.gov] Δ Glucagon remained unchanged (minutes 240 to 360; P 0.58) in TP/IAT recipients despite abnormal decreases in postprandial glucose.[ncbi.nlm.nih.gov] We present an infant with severe familial hyperinsulinism in whom glucose production rate, lipolysis, and gluconeogenesis from glycerol were measured by use of glucose and[ncbi.nlm.nih.gov] We report a 34-year old woman with familial partial lipodystrophy type 2 (Dunnigan) and diabetes; her hyperglycaemia persisted despite metformin treatment.[ncbi.nlm.nih.gov] This complication suggests abnormal input of autonomic nerves to the islets of pancreas in Johanson-Blizzard syndrome.[ncbi.nlm.nih.gov]

    Missing: OF WITH
  • Arsenic Trioxide

    In the course of this, LiCl induced inhibitory glycogen synthase kinase-3β (GSK-3β) serine 9 phosphorylation, whereas glioma associated oncogene family 1 (GLI1) protein expression[ncbi.nlm.nih.gov] The positive expression rate of ezrin in HCC was significantly higher than that in adjacent tissues, liver cirrhosis, and normal liver tissues.[journals.lww.com] Both are relatively rare secondary minerals found in oxidation zones of As-rich ore deposits.[en.wikipedia.org] Arsenic trioxide is known to cause electrocardiographic abnormalities, such as ventricular tachycardia and prolongation of QT interval.[ncbi.nlm.nih.gov] […] vitreous, amorphous form remains at the bottom of the tube) with the monoclinic form subliming onto the intermediate part of the tube at 200o (m 312o), and the octahedral form deposits[chemicalbook.com] Serious adverse effects that can occur include hyperleukocytosis, electrocardiographic abnormalities, and APL differentiation syndrome.[ncbi.nlm.nih.gov] Extracellular signal-regulated kinase 8 (ERK8), also known as mitogen-activated protein kinase 15 (MAPK15), is the most recently identified protein kinase of the ERK family[ncbi.nlm.nih.gov]

    Missing: OF WITH
  • Vicia Faba

    […] gels, water-soluble O-glycosyl polyacrylamide copolymers and polysaccharides were used. alpha-D-Galactosidases interact with immobilized O-alpha-D-galactosyl residues and glycogen[ncbi.nlm.nih.gov] We suggest that Vf might be of value in treating conditions such as hypertension, heart failure, renal failure, and liver cirrhosis in which natriuresis and diuresis are medically[ncbi.nlm.nih.gov] The mechanism of its antifungal action toward V. mali included (1) induction of alteration of hyphal morphology, (2) growth inhibition by chitin deposition at hyphal tips,[ncbi.nlm.nih.gov] […] obtained under transmission electron microscopy (TEM) further revealed apoptotic-like features at the ultrastructural level of PCC-type cells: (i) extensive vacuolization; (ii) abnormal[ncbi.nlm.nih.gov] Plant Groups Cacti and succulents identification Cacti Agavoideae (Agave subfamily) Asphodeloideae (Aloe family) Aizoaceae (Mesembs, Stone Plants, Living Stones) Euphorbiaceae[plantsam.com] Article - full text (enhanced PDF format, 3245255 bytes) Article sharing - repository deposits - copyright questions References How to cite this article Translate Download[actahort.org] ., 2015 ) in polarized wall ingrowth deposition.[frontiersin.org]

    Missing: OF WITH
  • Adrenal Insufficiency

    Cortisol and cortisone are referred to as glucocorticoid hormones because they cause conversion of amino acids and glycogen to glucose.[arltma.com] A 65-year-old male with liver cirrhosis of alcoholic etiology was admitted to hospital with bilateral leg edema, ascites, and marked weakness.[ncbi.nlm.nih.gov] Copper deposition or secondary neuronal damage in the pituitary may be a possible explanation for this theory.[ncbi.nlm.nih.gov] See glucocorticoid , mineralocorticoid , androgen . adrenal cortex inhibitors adrenal cortical dysfunction adrenal hyperplasia-like syndrome a congenital abnormality of adrenal[medical-dictionary.thefreedictionary.com] Families should receive education on managing illness or stress, that is, steroid sick day rules. Most of this education is delivered by children's nurses.[ncbi.nlm.nih.gov] Calcium deposits may indicate TB. A tuberculin skin test also may be used.[pituitary.org] […] hemorrhage (e.g. in Waterhouse-Friderichsen syndrome or antiphospholipid syndrome ), particular infections ( tuberculosis , histoplasmosis , coccidioidomycosis ), or the deposition[en.wikipedia.org]

    Missing: OF WITH
  • Gout

    A search of the previous literature revealed 16 reported cases of glycogen storage disease type Ia with gout.[ncbi.nlm.nih.gov] Alterations of the human gut microbiome in liver cirrhosis . Nature 513 , 59–64 (2014). 27. Qin, J. J. et al.[nature.com] The frequency of urate crystal deposition detected by US at MTP1, knee, and ankle joints regions was 56.7%, 63.3%, and 51.7%, respectively.[ncbi.nlm.nih.gov] Among controls, 16% were found to have these abnormal ultrasound findings by both two sites and six sites examinations.[ncbi.nlm.nih.gov] We report 2 cases of familial juvenile hyperuricemic nephropathy, a rare autosomal dominant disorder characterized by uromodulin gene mutations leading to hyperuricemia secondary[ncbi.nlm.nih.gov] We studied clinical, biochemical and molecular genetic characteristics of Czech families with hyperuricemia and HPRT deficiency.[ncbi.nlm.nih.gov] Gout, a common and complex form of inflammatory arthritis, is characterized by abnormally elevated levels of uric acid in the blood.[ncbi.nlm.nih.gov]

    Missing: OF WITH
  • Wilson Disease

    We found that 29 patients (88%) showed glycogenated hepatocyte nuclei and 27 patients (79%) showed nuclear pleomorphism.[ncbi.nlm.nih.gov] Liver cirrhosis can also lead to accumulation of neurotoxins causing hepatic encephalopathy.[ncbi.nlm.nih.gov] It is currently unknown whether this hypointensity is related to copper or iron deposition.[ncbi.nlm.nih.gov] Out of 51 patients 22 had at least one ECG abnormality.[ncbi.nlm.nih.gov] We recently evaluated a Korean family with WD.[ncbi.nlm.nih.gov] Additional findings include liver cell degeneration and ballooning, Mallory hyaline bodies, liver cell necrosis, and glycogenation of periportal hepatocytic nuclei.[ncbi.nlm.nih.gov] Microscopic (histologic) images Images hosted on PathOut server: Case of the Week #388: Rhodanine stain for copper Electron microscopy description Microvesicular steatosis, glycogen[pathologyoutlines.com]

    Missing: OF WITH
  • Secondary Amyloidosis

    We observed the development of generalized amyloidosis in a girl with glycogen storage disease type Ib (GSD-Ib) who showed neutropenia, neutrophil dysfunction and recurrent[ncbi.nlm.nih.gov] As a workup for secondary amyloidosis, her liver biopsy was done which revealed features of primary billiary cirrhosis (PBC).[ncbi.nlm.nih.gov] No other organs or tissues were surveyed for amyloid deposition.[ncbi.nlm.nih.gov] We demonstrated that majority of the patients with secondary amyloidosis had serum lipid abnormalities.[ncbi.nlm.nih.gov] Familial Mediterranean fever (FMF) is an inflammatory disorder that is leading cause of secondary amyloidosis (AA).[ncbi.nlm.nih.gov] Review of the Published and Unpublished Data of the Randomized Double-Blind SMILE-4 Study Articolo su rivista Vai 2018 Subclinical cardiovascular damage in patients with HCV cirrhosis[unipa.it] The family history was positive in 16%; 73% of the cases were on colchicine treatment when the questionnaire was administered.[ncbi.nlm.nih.gov]

    Missing: OF WITH
  • Olecranon Bursitis

    […] from erosion of long-standing soft-tissue tophus "Overhanging margin" (40%) Ischemic necrosis of femoral / humeral heads Bone infarction Coexisting disorders: Psoriasis Glycogen[learningradiology.com] Cirrhosis may be an independent risk factor because of impaired chemotaxis and phagocytosis.[ncbi.nlm.nih.gov] It is concluded that bursitis may be part of the extraarticular manifestations of calcium pyrophosphate dihydrate crystal deposition disease.[ncbi.nlm.nih.gov] […] nutritional and metabolic diseases ( E00 - E88 ) injury, poisoning and certain other consequences of external causes ( S00-T88 ) neoplasms ( C00-D49 ) symptoms, signs and abnormal[icd10data.com] A previously healthy 72-year-old man fell from a stationary bicycle and was examined by his family physician.[ncbi.nlm.nih.gov] In addition, small apatite deposits were observed in the bursa and tendon by electron microscopy.[ncbi.nlm.nih.gov] Blahd, Jr., MD, FACEP - Emergency Medicine & Adam Husney, MD - Family Medicine & Kathleen Romito, MD - Family Medicine[uofmhealth.org]

    Missing: OF WITH
  • Familial Hypercholesterolemia

    Disorders in Children and Adolescents 478 Thyroid Cancer in Children 507 Hypoglycemia in Adults 526 Obesity 545 Disorders of Lipid Metabolism 554 INBORN ERRORS OF METABOLISM 568 Glycogen[books.google.de] A 46-yr-old female with hepatocellular carcinoma and severe hepatitis B-related liver cirrhosis received a domino liver graft from a 25-yr-old female with homozygous familial[ncbi.nlm.nih.gov] In this study, we report a homozygous LDLR mutation (c.298G A) in a familial hypercholesterolemia patient, who exhibited intracranial cholesterol deposition, which is a rare[ncbi.nlm.nih.gov] Several studies in FH patients have pointed to the qualitative abnormalities of high-density lipoprotein (HDL) particles, including their triglyceride and sphingomyelin enrichment[ncbi.nlm.nih.gov] Type 2B: Familial combined hyperlipidemia Type 3: Familial dysbetalipoproteinemia or hyperlipoproteinemia type 3 Type 4: Familial hypertriglyceridemia Type 5: Primary mixed[symptoma.com] Disease Type IXa1 3 Glycogen Storage Disease Type IXc 3 Glycogen Storage Disease Type IXd 3 Glycogen Storage Disease Type V 6 Glycogen Storage Disease Type VI 3 Glycogen[preventiongenetics.com] , we report a case of domino liver transplantation using the liver of a 14-year-old boy with homozygous FH into a 65-year-old man with primary sclerosing cholangitis and cirrhosis[ncbi.nlm.nih.gov]

    Missing: OF WITH

Similar symptoms