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16 Possible Causes for Early-Onset Hepatocellular Carcinoma

  • Ruijs Aalfs Syndrome

    In addition, both brothers developed early-onset hepatocellular carcinoma, at ages 16 and 14 years, respectively.[ncbi.nlm.nih.gov]

  • Hepatocellular Carcinoma

    Blasco, Mice lacking RAP1 show early onset and higher rates of DEN-induced hepatocellular carcinomas in female mice, PLOS ONE, 10.1371/journal.pone.0204909, 13, 10, (e0204909[doi.org] Evaluation of current guidelines for hepatocellular carcinoma In the past 10 years, many guidelines for HCC have been published worldwide since the European Association for[hepatitiscresearchandnewsupdates.blogspot.com.es] Tamara Severi, Hannah van Malenstein, Chris Verslype and Jos F van Pelt, Tumor initiation and progression in hepatocellular carcinoma: risk factors, classification, and therapeutic[doi.org]

  • Combined Oxidative Phosphorylation Defect Type 14

    carcinoma, childhood-onset Hereditary coproporphyria Hereditary motor and sensory neuropathy, Okinawa type Hereditary orotic aciduria Hereditary proximal myopathy with early[csbg.cnb.csic.es] […] deficiency Glycogen storage disease due to muscle phosphofructokinase deficiency HSD10 disease, atypical type HSD10 disease, infantile type HSD10 disease, neonatal type Hepatocellular[csbg.cnb.csic.es]

  • Alagille Syndrome

    Because of the unusual liver histology and early onset of hepatocellular carcinoma, careful clinicopathologic correlations and close monitoring are required for the diagnosis[ncbi.nlm.nih.gov] Eventually, all three cases progressed to biliary cirrhosis and hepatocellular carcinoma, which occurred at 17 months, 4 years, and 7 years, respectively.[ncbi.nlm.nih.gov] […] of Alagille syndrome and for the early detection of hepatocellular carcinoma.[ncbi.nlm.nih.gov]

  • Alpha-1 Antichymotrypsin Deficiency

    Lung disease may progress to early-onset lower lobe emphysema. Additional Reading Miranda E, Pérez J, Ekeowa UI, et al.[unboundmedicine.com] Complications Patients with liver disease may develop complications of chronic liver disease including portal hypertension, cirrhosis, and/or hepatocellular carcinoma.[unboundmedicine.com]

  • Autosomal Recessive Spastic Paraplegia Type 39

    DPM1-CDG Early-onset autosomal dominant Alzheimer disease Familial isolated hyperparathyroidism Familial papillary renal cell carcinoma Familial parathyroid adenoma Familial[csbg.cnb.csic.es] […] prostate cancer Familial short QT syndrome Gitelman syndrome Hepatocellular carcinoma, childhood-onset Hereditary breast cancer Hereditary cerebral hemorrhage with amyloidosis[csbg.cnb.csic.es] […] dominant secondary polycythemia Autosomal dominant spastic paraplegia type 13 Bardet-Biedl syndrome CLN4B disease Cabezas syndrome Chuvash erythrocytosis Clear cell renal carcinoma[csbg.cnb.csic.es]

  • Tyrosinemia

    HTI is characterized by progressive liver dysfunction with nodular cirrhosis often leading to hepatocellular carcinoma.[ncbi.nlm.nih.gov] Two extremes of the clinical phenotype have been described: the "acute" (severe, early onset and death) and "chronic" (delayed onset and slow course) phenotype.[ncbi.nlm.nih.gov]

  • Hypomandibular Faciocranial Dysostosis

    carcinoma (fibrolamellar variant) Hepatocellular carcinoma adult Hepatocellular carcinoma childhood Hepatoerythropoietic porphyria Hepatorenal syndrome Hereditary amyloidosis[personalizedcause.com] Hereditary angioedema Hereditary ataxia Hereditary cerebellar ataxia syndrome of early onset Hereditary cerebral hemorrhage with amyloidosis Hereditary congenital facial[personalizedcause.com] […] encephalopathy Hepatic fibrosis renal cysts mental retardation Hepatic venoocclusive disease with immunodeficiency Hepatitis E Hepatitis X (non-A -B -C -D -E) Hepatoblastoma Hepatocellular[personalizedcause.com]

  • Neurofibromatosis Type 3

    carcinoma, childhood-onset Pilomatrixoma Early-onset autosomal dominant Alzheimer disease Hereditary cerebral hemorrhage with amyloidosis, Arctic type Hereditary cerebral[csbg.cnb.csic.es] […] mycobacterial diseases due to IKBKG deficiency Autosomal dominant nonsyndromic intellectual deficit Brachydactyly type A2 Brachydactyly type C Craniopharyngioma Desmoid tumor Hepatocellular[csbg.cnb.csic.es]

  • Autosomal Dominant Non-Syndromic Intellectual Disability

    […] fragility-woolly hair-palmoplantar keratoderma syndrome Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome Behavioral variant of frontotemporal dementia Early-onset[csbg.cnb.csic.es] carcinoma, childhood-onset Pilomatrixoma Estrogen resistance syndrome Giant cell glioblastoma Gliosarcoma EEM syndrome Hypotrichosis with juvenile macular degeneration Hereditary[csbg.cnb.csic.es] […] non-fluent aphasia Semantic dementia Autosomal dominant medullary cystic kidney disease with or without hyperuricemia Split hand-split foot malformation Craniopharyngioma Hepatocellular[csbg.cnb.csic.es]

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