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130 Possible Causes for Mild Elevation of Triglycerides, Mutation in the CALM2 Gene

  • Glycogen Storage Disease due to Muscle Phosphorylase Kinase Deficiency

    Clinical manifestations of the patient carrying this mutation were reported to include growth delay, mild fasting hypoglycemia, post-prandial lactatemia, and elevated serum[bmcmedgenet.biomedcentral.com] There are autosomal recessive forms of GSD IX (caused by mutations in PHKB, PHKG1, PHKG2, CALM1, CALM2, and CALM3 ), a X-linked liver form (caused by mutations in PHKA2 ),[bmcmedgenet.biomedcentral.com] triglycerides, with age at onset of 9 months [ 6 ].[bmcmedgenet.biomedcentral.com]

  • Phosphorylase Kinase Deficiency

    Clinical manifestations of the patient carrying this mutation were reported to include growth delay, mild fasting hypoglycemia, post-prandial lactatemia, and elevated serum[bmcmedgenet.biomedcentral.com] There are generally mild ketosis, growth retardation, prominent hepatomegaly and elevated levels of serum transaminases, triglycerides and cholesterol[ 124 ], although biochemical[wjgnet.com] There are autosomal recessive forms of GSD IX (caused by mutations in PHKB, PHKG1, PHKG2, CALM1, CALM2, and CALM3 ), a X-linked liver form (caused by mutations in PHKA2 ),[bmcmedgenet.biomedcentral.com]

  • Hypertension

    Obesity is commonly associated with a combined dyslipidemia pattern with mild elevation in TC and LDL cholesterol levels, moderate-to-severe elevation in triglyceride level[doi.org] Since then, the predominant dyslipidemic pattern in childhood is a combined pattern associated with obesity, moderate-to-severe elevation in triglyceride level, normal-to-mild[doi.org] elevation in LDL cholesterol level, and a reduced HDL cholesterol level.[doi.org]

    Missing: Mutation in the CALM2 Gene
  • Acne Vulgaris

    Isotretinoin can also be associated with a mild to moderate elevation in liver enzymes and in serum lipid indices, especially triglycerides. 87 It is generally well accepted[jamanetwork.com]

    Missing: Mutation in the CALM2 Gene
  • Hypoglycemia

    GSD IV (Hers disease): Typical scenario : Mild-moderate hypoglycemia, hepatomegaly and FTT in infants, sometimes slight liver enzyme, triglyceride and cholesterol elevation[pedclerk.bsd.uchicago.edu]

    Missing: Mutation in the CALM2 Gene
  • Insulin Resistance

    Initially there is only mild rise in blood glucose, we call it Pre-diabetes. Later there is higher elevation in blood glucose which we call as diabetes.[onlinemedinfo.com] Insulin resistance also causes a high level of triglycerides and a low level of HDL (good) cholesterol.[onlinemedinfo.com]

    Missing: Mutation in the CALM2 Gene
  • Hyponatremia

    Elevated triglyceride or cholesterol levels, immunoglobulins, and monoclonal gammopathies—through laboratory artifacts—may all cause falsely low serum Na concentrations without[content.onlinejacc.org] This may not be necessary when hyponatremia is mild (serum Na concentration 130 to 134 mEq), asymptomatic, and easily corrected by empiric treatment.[content.onlinejacc.org]

    Missing: Mutation in the CALM2 Gene
  • Glycogen Storage Disease due to Liver Phosphorylase Kinase Deficiency

    Clinical manifestations of the patient carrying this mutation were reported to include growth delay, mild fasting hypoglycemia, post-prandial lactatemia, and elevated serum[bmcmedgenet.biomedcentral.com] There are generally mild ketosis, growth retardation, prominent hepatomegaly and elevated levels of serum transaminases, triglycerides and cholesterol[ 124 ], although biochemical[wjgnet.com] There are autosomal recessive forms of GSD IX (caused by mutations in PHKB, PHKG1, PHKG2, CALM1, CALM2, and CALM3 ), a X-linked liver form (caused by mutations in PHKA2 ),[bmcmedgenet.biomedcentral.com]

  • Renal Colic

    Laboratory tests showed normal creatinine, mild reduction of albuminemia, elevated triglycerides and cholesterol at the upper limit of normal.[ncbi.nlm.nih.gov]

    Missing: Mutation in the CALM2 Gene
  • Long QT Syndrome 15

    エントリ H00720 名称 QT 延長症候群 下位グループ ロマノワード症候群 ジャーベル・ランゲ・ニールセン症候群 [DS: H02091 ] 概要 QT 延長症候群は心電図の QT 間隔の異常な延長と失神発作を示す心血管障害である。他の疾患や薬物の影響で起こる後天性と、心筋細胞のイオンチャネルをコードする遺伝子の異常による先天性がある。発作のないときは無症状であるが、発作時はトルサド・ド・ポアンツ (Tdp) と呼ばれる心室性不整脈を特徴とし、適切な医療処置を行わないと心室細動に移行して死亡することもある。QT[…][genome.jp]

    Missing: Mild Elevation of Triglycerides

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