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109 Possible Causes for Hypoinsulinemic Hypoglycemia

  • Hypoglycemia

    […] hypoglcyemia) and those with appropriately low insulin levels (hypoinsulinemic hypoglycemia).[clinicaladvisor.com] In the case of hypoinsulinemic hypoglycemia, deficiencies of cortisol and/or growth hormone are sometimes cited as potential explanations.[clinicaladvisor.com] In patients with symptoms whose blood glucose is genuinely low, there are two major types of hypoglycemia: those with inappropriately high insulin levels (hyperinsulinemic[clinicaladvisor.com]

  • Hypoinsulinemic Hypoglycemia and Body Hemihypertrophy

    DISEASE: Hypoinsulinemic hypoglycemia with hemihypertrophy Entry H01909 Disease Name Hypoinsulinemic hypoglycemia with hemihypertrophy Description Hypoinsulinemic hypoglycemia[genome.jp] Homepage Rare diseases Search Search for a rare disease Hypoinsulinemic hypoglycemia and body hemihypertrophy Disease definition Hypoinsulinemic hypoglycemia and body hemihypertrophy[orpha.net] Test Directory & Ordering - Clinical Synopsis HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY; HIHGHH Custom clinical synopsis deleted successfully.[mnglabs.com]

  • Islet Cell Tumor

    These data suggested that hypoinsulinemic hypoglycemia associated with the presence of a large tumor supports the diagnosis of IGF-II producing NICTH.[ncbi.nlm.nih.gov] Hypoglycemic attack was the onset of disease in 31 of 65 cases (48%), but the tumor was revealed prior to the occurrence of hypoglycemia in 34 cases (52%).[ncbi.nlm.nih.gov]

  • Dilated Cardiomyopathy Type 2B

    Long QT syndrome-11 611820 604001 Autosomal dominant AKT2 19q13.2 Hypoinsulinemic hypoglycemia with hemihypertrophy 240900 164731 Autosomal dominant AKT2 19q13.2 Diabetes[mnglabs.com]

  • Young Adult-Onset Distal Hereditary Motor Neuropathy

    hypoglycemia and body hemihypertrophy Hypoplastic left heart syndrome Hypotonia with lactic acidemia and hyperammonemia Hypoxanthine guanine phosphoribosyltransferase partial[csbg.cnb.csic.es] […] nonpolyposis colon cancer Hereditary sensory and autonomic neuropathy type 1 Hermansky-Pudlak syndrome with neutropenia Herpetic encephalitis Hoyeraal-Hreidarsson syndrome Hypoinsulinemic[csbg.cnb.csic.es]

  • Early-Onset Autosomal Dominant Alzheimer Disease

    hypoglycemia and body hemihypertrophy Pelizaeus-Merzbacher-like due to HSPD1 mutation CADDS Follicular lymphoma Intravascular large B-cell lymphoma Peters anomaly Severe[csbg.cnb.csic.es] […] myopathy Zonular cataract Familial amyloidosis, Finnish type Acatalasemia Autosomal dominant spastic paraplegia type 13 Familial partial lipodystrophy due to AKT2 mutations Hypoinsulinemic[csbg.cnb.csic.es]

  • Macrocephaly

    Gene Prevalence Penetrance Clinical sensitivity Inheritance Condition AKT2 rare, unknown unknown unknown AD Hypoinsulinemic hypoglycemia with hemihypertrophy AKT3 rare, unknown[invitae.com] Intellectual disability syndrome with central obesity, macrocephaly and macrosomic features epiphyseal chondrodysplasia, Miura type ( ECDM ) Greig cephalopolysyndactyly syndrome hypoinsulinemic[invitae.com] hypoglycemia with hemihypertrophy Legius syndrome Lujan-Fryns syndrome Luscan-Lumish syndrome megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 1 megalencephaly-polymicrogyria-polydactyly-hydrocephalus[invitae.com]

  • Deafness, Autosomal Dominant 23

    Long QT syndrome-11 611820 604001 Autosomal dominant AKT2 19q13.2 Hypoinsulinemic hypoglycemia with hemihypertrophy 240900 164731 Autosomal dominant AKT2 19q13.2 Diabetes[mnglabs.com]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2U

    Long QT syndrome-11 611820 604001 Autosomal dominant AKT2 19q13.2 Hypoinsulinemic hypoglycemia with hemihypertrophy 240900 164731 Autosomal dominant AKT2 19q13.2 Diabetes[mnglabs.com]

  • Glycogen Storage Disease due to Phosphoglycerate Kinase 1 Deficiency

    hypoglycemia with hemihypertrophy ALAD Porphyria, acute hepatic ALAS2 Anemia, sideroblastic, Protoporphyria, erythropoietic ALDH5A1 Succinic semialdehyde dehydrogenase deficiency[genda.com.ar] hypoglycemia with hemihypertrophy BSCL2 Encephalopathy, progressive, Lipodystrophy, congenital generalized CAV1 Lipodystrophy, congenital generalized, Partial lipodystrophy[genda.com.ar] Spinocerebellar ataxia ADSL Adenylosuccinase deficiency AGA Aspartylglucosaminuria AGK Sengers syndrome AGL Glycogen storage disease AGPAT2 Lipodystrophy, congenital generalized AKT2 Hypoinsulinemic[genda.com.ar]

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