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16 Possible Causes for CONGEN, Hypocupremia

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  • Menkes Disease

    RCG040 DIFETTI CONGENITI DEL METABOLISMO E DEL TRASPORTO DEGLI AMINOACIDI FENILCHETONURIA/IPERFENILALANINEMIA TIROSINEMIA ISTIDINEMIA ALCAPTONURIA LEUCINOSI (MALATTIA DELLE[www1.unipa.it] MENKES DISEASE – CLASSIC or INFANTILE ONSET FORM ALTERNATE NAMES Classical Menkes Disease; Menkes Syndrome ; X-linked Copper Deficiency; Steely Hair Disease; Congenital Hypocupremia[secure.ssa.gov] Copper transport disease Hypocupremia, Congenital Kinky Hair Syndrome Menkea syndrome Menkes Disease MK MNK Steely Hair Syndrome X-linked copper deficiency Barnes N, Tsivkovskii[ghr.nlm.nih.gov]

  • Disorder of Copper Metabolism

    RCG040 DIFETTI CONGENITI DEL METABOLISMO E DEL TRASPORTO DEGLI AMINOACIDI FENILCHETONURIA/IPERFENILALANINEMIA TIROSINEMIA ISTIDINEMIA ALCAPTONURIA LEUCINOSI (MALATTIA DELLE[www1.unipa.it] […] disease Or: 2015/16 ICD-10-CM E83.09 Other disorders of copper metabolism Approximate Synonyms Copper deficiency Copper metabolism disorder Disorder of copper metabolism Hypocupremia[icd9data.com] Low blood copper concentrations (hypocupremia) are seen in malabsorption syndromes, increased zinc consumption, patients following gastric bypass surgery, patients on prolonged[selfhacked.com]

  • Brandt Syndrome

    RCG040 DIFETTI CONGENITI DEL METABOLISMO E DEL TRASPORTO DEGLI AMINOACIDI FENILCHETONURIA/IPERFENILALANINEMIA TIROSINEMIA ISTIDINEMIA ALCAPTONURIA LEUCINOSI (MALATTIA DELLE[www1.unipa.it] Most authors recommend an initial zinc supplementation at the dose of 5–10 mg/kg/day and maintenance with 1–2 mg/kg/day. [5] High serum levels of zinc lead to hypocupremia[ijpd.in] Side effects are gastric irritation, gastric hemorrhage and hypocupremia. [1] This case is being reported to highlight that isolated zinc deficiency can occur in adults and[e-ijd.org]

  • Erythrocytosis

    […] glomerulonephritis and post renal transplantation Familial mutations in the erythropoietin receptor or 2,3-bisphosphoglycerate (2,3-BPG) Certain drugs such as testosterone and its congeners[oncologynurseadvisor.com] Diff dx: Iron deficiency (95%), Beta thalassemia trait, anemia of chronic disease, Refractory anemia w/ ringed sideroblasts (MDS), Lead poisoning, Alpha thalassemia trait, Hypocupremia[quizlet.com]

  • Secondary Optic Atrophy

    LINFOCITARIA CRONICA Coloro che sono già esenti per le seguenti malattie: Angioedema ereditario, Dermatomiosite, Pemfigo e pemfigoidi, Anemie congenite, Fenilchetonuria ed errori congeniti[sanalimentazione.it] CNS demyelination due to hypocupremia in Wilson's disease from overzealous treatment. Neurol India 2006;54:110-1. [ PUBMED ][neurologyindia.com] It is crucial to elicit a history of gastric surgery or other risk factors for hypocupremia in patients undergoing evaluation for subacute or chronically progressive optic[neurologyindia.com]

  • Familial Hyperaldosteronism Type 3

    CONGENITI DEL METABOLISMO E DEL TRASPORTO DELLA VITAMINA D (RCG094) RACHITISMO VITAMINA D DIPENDENTE TIPO I (RCG095) ALTRI DIFETTI CONGENITI DEL METABOLISMO E DEL TRASPORTO[malattierare.toscana.it] […] hypercalcemia, type 2 - See Familial hypocalciuric hypercalcemia type 2 Familial benign hypercalcemia, type 3 - See Familial hypocalciuric hypercalcemia type 3 Familial benign hypocupremia[rarediseases.info.nih.gov] DI CITOCROMO C OSSIDASI (RCG077) DIFETTI CONGENITI ISOLATI DI UN COMPLESSO DELLA FOSFORILAZIONE OSSIDATIVA MITOCONDRIALE (RCG078) DIFETTI CONGENITI DELLA FOSFORILAZIONE OSSIDATIVA[malattierare.toscana.it]

  • Tangier Disease

    RCG040 DIFETTI CONGENITI DEL METABOLISMO E DEL TRASPORTO DEGLI AMINOACIDI FENILCHETONURIA/IPERFENILALANINEMIA TIROSINEMIA ISTIDINEMIA ALCAPTONURIA LEUCINOSI (MALATTIA DELLE[www1.unipa.it] 815,70 Hyphäma, 0,11, 0,57, 0,95, 5,50, 217.50, 117.50, 162.50, 393.50, 677,91, 797,61 Hypochondrie, 0,03, 0,50, 0,85, 7,50, 8,00, 127,50, 235,58, 525,79, 725,00, 825,79 Hypocupremia[rifeandzappers2.com] IPERINSULINISMO CONGENITO DA DEFICIT DI GLUCOCHINASI RCG070 DIFETTI CONGENITI DEL METABOLISMO DELLE LIPOPROTEINE (Escluso: Ipercolesterolemia familiare eterozigote tipo IIa[www1.unipa.it]

  • Non-Syndromic Aplasia Cutis Congenita

    CONGENITI DELL'ASSORBIMENTO E DEL TRASPORTO DI VITAMINE E COFATTORI NON PROTEICI DIFETTI CONGENITI DEL METABOLISMO E DEL TRASPORTO DI METALLI8/26 elenco MR esentate dalla[dokumen.tips] 815,70 Hyphäma, 0,11, 0,57, 0,95, 5,50, 217.50, 117.50, 162.50, 393.50, 677,91, 797,61 Hypochondrie, 0,03, 0,50, 0,85, 7,50, 8,00, 127,50, 235,58, 525,79, 725,00, 825,79 Hypocupremia[rifeandzappers2.com] DEL METABOLISMO E DEL TRASPORTO DELLE PROTEINE RCG103 RCG102 RCG101 RCG100 DIFETTI CONGENITI DEL METABOLISMO E DEL TRASPORTO DI METALLI ALTRI DIFETTI CONGENITI DEL METABOLISMO[dochero.tips]

  • Leukoencephalopathy - Metaphyseal Chondrodysplasia Syndrome

    LINFOCITARIA CRONICA Coloro che sono già esenti per le seguenti malattie: Angioedema ereditario, Dermatomiosite, Pemfigo e pemfigoidi, Anemie congenite, Fenilchetonuria ed errori congeniti[sanalimentazione.it] […] retardation epilepsy Mental retardation epilepsy bulbous nose Mental retardation gynecomastia obesity X-linked Mental retardation hip luxation G6PD variant Mental retardation hypocupremia[diseaseinfosearch.org]

  • Mandibuloacral Dysostosis

    LINFOCITARIA CRONICA Coloro che sono già esenti per le seguenti malattie: Angioedema ereditario, Dermatomiosite, Pemfigo e pemfigoidi, Anemie congenite, Fenilchetonuria ed errori congeniti[sanalimentazione.it] […] retardation epilepsy Mental retardation epilepsy bulbous nose Mental retardation gynecomastia obesity X-linked Mental retardation hip luxation G6PD variant Mental retardation hypocupremia[personalizedcause.com]

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