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160 Possible Causes for Transient Hypertriglyceridemia

  • Insulin Resistance

    Abstract Biallelic mutations in the GPD1 gene cause a rare autosomal recessive inherited disease known as transient infantile hypertriglyceridemia (OMIM #614480).[ncbi.nlm.nih.gov]

  • Psoriasis

    Mild elevations in transaminases are rarely seen 2 to 8 weeks after the start of acitretin, but these are transient and just require monitoring. 73 Checking the following[doi.org] […] cholesterol levels 300 mg/dL warrant a discontinuation of acitretin and close monitoring of lipids until they return to baseline. 73 Sometimes, a fenofibrate is recommended for hypertriglyceridemia[doi.org]

  • Familial Hypercholesterolemia

    Plasma transfusions may transiently help patients with APOC2 mutations. Gemfibrozil in the 3 rd trimester in pregnancy in HLP type 1. Apheresis is of questionable value.[mdpi.com] Acute pancreatitis with severe hypertriglyceridemia - NPO - Supportive measures - Address secondary or exacerbating factors such as alcohol intake or glycemic control - When[mdpi.com]

  • Transient Infantile Hypertriglyceridemia and Hepatosteatosis

    OMIM : 57 Transient infantile hypertriglyceridemia is an autosomal recessive disorder characterized by onset of moderate to severe transient hypertriglyceridemia in infancy[malacards.org] Symptoms of Hypertriglyceridemia, transient infantile Clinical features : Imported from Human Phenotype Ontology (HPO) Abnormality of metabolism/homeostasis Hypertriglyceridemia[familydiagnosis.com] , transient infantile (HTGTI) [MIM:614480]: An autosomal recessive disorder characterized by onset of moderate to severe transient hypertriglyceridemia in infancy that normalizes[genecards.org]

  • Hereditary North American Indian Childhood Cirrhosis

    […] familial neonatal hyperbilirubinemia Transient infantile hypertriglyceridemia and hepatosteatosis Tyrosinemia type 1 Wilson disease Zellweger syndrome[se-atlas.de] […] liver disease Rare vascular liver disease Reynolds syndrome Rotor syndrome Solitary necrotic nodule of the liver Steroid dehydrogenase deficiency-dental anomalies syndrome Transient[se-atlas.de]

  • Transient Familial Neonatal Hyperbilirubinemia

    […] neonatal hypertriglyceridemia and hypercholesterolemia are excluded.[pediatrics.aappublications.org] […] familial neonatal hyperbilirubinemia Transient infantile hypertriglyceridemia and hepatosteatosis Tyrosinemia type 1 Wilson disease Zellweger syndrome[se-atlas.de] […] is concluded that the measurement of prebeta-β-lipoprotein in cord serum allows the identification of children with familial type II hyperlipoproteinemia, if infants with transient[pediatrics.aappublications.org]

  • Generalized Epilepsy with Febrile Seizures Plus

    , Transient Infantile Hypertriglyceridemia GPD1L glycerol-3-phosphate dehydrogenase 1-like 3p22.3 Brugada Syndrome 2, Right Bundle Branch Block, Sudden Infant Death Syndrome[genecards.weizmann.ac.il] Postaxial Polydactyly, Type A2 Anoxia Show all 6 GPC6 glypican 6 13q31.3 Omodysplasia 1 Body Dysmorphic Disorder GPD1 glycerol-3-phosphate dehydrogenase 1 (soluble) 12q13.12 Hypertriglyceridemia[genecards.weizmann.ac.il]

  • Dilated Cardiomyopathy Type 2B

    , transient infantile 614480 138420 Autosomal recessive GPD1L 3p22.3 Brugada syndrome 2 611777 611778 GPD2 2q24.1 {Diabetes, type 2, susceptibility to} 125853 138430 Autosomal[mnglabs.com] […] type 1 312870 300037 X-linked recessive GPC3 Xq26.2 Wilms tumor, somatic 194070 300037 GPC6 13q31.3-q32.1 Omodysplasia 1 258315 604404 Autosomal recessive GPD1 12q13.12 Hypertriglyceridemia[mnglabs.com]

  • Diabetic Ketoacidosis

    In cases of acute pancreatitis during DKA, transient hypertriglyceridemia is postulated to be the primary etiology[ 68, 71 ] through both increased blood viscosity and increased[doi.org]

  • Fatty Liver

    Abstract Biallelic mutations in the GPD1 gene cause a rare autosomal recessive inherited disease known as transient infantile hypertriglyceridemia (OMIM #614480).[ncbi.nlm.nih.gov]

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