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1,426 Possible Causes for Cognitive Developmental Delay, Kussmaul Respiration, Persistent Lactic Acidosis

  • Acidosis

    Hyperlactatemia is defined as a persistent, mild to moderate (2-4 mmol/L) increase in blood lactate concentration without metabolic acidosis , whereas lactic acidosis is characterized[emedicine.medscape.com] ., dyspnea, marked Kussmaul respirations) These patients generally have severe metabolic acidosis with respiratory compensation.[emcrit.org] respiration E87.2 Lacticemia, excessive E87.2 Retention - see also Retained carbon dioxide E87.2 ICD-10-CM Codes Adjacent To E87.2 E85.82 Wild-type transthyretin-related[icd10data.com]

    Missing: Cognitive Developmental Delay
  • Lactic Acidosis

    […] interval: 2.5-20.6; P CONCLUSION: In the absence of risk factors associated with persistent lactic acidosis, such as shock or acute kidney or liver injury, continued peri-operative[ncbi.nlm.nih.gov] lactic acidosis CAUSES (Cohen & Woods classification) Type A – Inadequate Oxygen Delivery anaerobic muscular activity (sprinting, generalised convulsions) tissue hypoperfusion[lifeinthefastlane.com] Multivariable logistic regression analysis identified the need for vasopressor administration as an independent predictor of lactic acidosis (odds ratio: 7.3, 95% confidence[ncbi.nlm.nih.gov]

    Missing: Cognitive Developmental Delay
  • Amish Lethal Microcephaly

    lactic acidosis Hand muscle weakness Delayed speech and language development Wide nasal bridge Axial muscle weakness Long philtrum Abnormality of the genital system Gowers[mendelian.co] developmental delays; short heights; and skeletal abnormalities.Lifespan is average in length, though.[owlcation.com] […] joint contracture Hypoventilation Shoulder girdle muscle weakness Central hypotonia Primitive reflex Abnormal posturing Biventricular hypertrophy Reduced ejection fraction Persistent[mendelian.co]

    Missing: Kussmaul Respiration
  • Mitochondrial Complex 3 Deficiency

    In addition, patients do not develop severe metabolic crises in the neonatal period as observed in other organic acidurias, but may show persistent lactic acidosis, most likely[mendelian.co]

    Missing: Kussmaul Respiration
  • Iron Deficiency

    The latter include decreased aerobic work performance, hair loss, developmental delay, cognitive and intellectual impairment, adverse pregnancy outcome, and impaired immune[www2.gov.bc.ca] Reversal of developmental delays in iron-deficient anaemic infants treated with iron. Lancet 1993;341(8836):1-4. Lozoff B, Jimenez E, Wolf AW.[cdc.gov] Iron deficiency and cognitive function. Annu Rev Nutr 1993;13:521-37. Idjradinata P, Pollitt E.[cdc.gov]

    Missing: Kussmaul Respiration Persistent Lactic Acidosis
  • Seckel Syndrome

    クスマウル Kussmaul respiration クスマウル大呼吸 AdolfKussmaul (1822-1902) Germaninternist Kveim クベイム反応 Kveim reaction クベイム反応 MortenAnsgar Kveim (1892-1966) Norwegian pathologist Ladd[jams.med.or.jp] German gynecologist and pathologist Kugelberg-Welander クーゲルベルク・ウェランダー Kugelberg-Welander disease クーゲルベルク・ウェランダー病 Kunitz クニッツ Kunitz soybean trypsin inhibitor クニッツ大豆トリプシン阻害物質 Kussmaul[jams.med.or.jp]

    Missing: Persistent Lactic Acidosis
  • Hartnup Disease

    クスマウル Kussmaul respiration クスマウル大呼吸 AdolfKussmaul (1822-1902) Germaninternist Kveim クベイム反応 Kveim reaction クベイム反応 MortenAnsgar Kveim (1892-1966) Norwegian pathologist Ladd[jams.med.or.jp] German gynecologist and pathologist Kugelberg-Welander クーゲルベルク・ウェランダー Kugelberg-Welander disease クーゲルベルク・ウェランダー病 Kunitz クニッツ Kunitz soybean trypsin inhibitor クニッツ大豆トリプシン阻害物質 Kussmaul[jams.med.or.jp]

    Missing: Persistent Lactic Acidosis
  • Waardenburg Syndrome Type 2E

    […] nonpersistance ( MCM6) Lactic acidosis, fatal infantile ( SUCLG1) Lacticacidemia due to PDX1 deficiency ( PDX1) LADD syndrome ( FGF10) LADD syndrome ( FGFR3) Laing distal[en.praenatal-medizin.de] クスマウル Kussmaul respiration クスマウル大呼吸 AdolfKussmaul (1822-1902) Germaninternist Kveim クベイム反応 Kveim reaction クベイム反応 MortenAnsgar Kveim (1892-1966) Norwegian pathologist Ladd[jams.med.or.jp] COL18A1) Kowarski syndrome ( GH1) Krabbe disease ( GALC) Krabbe disease, atypical ( PSAP) L-2-hydroxyglutaric aciduria ( L2HGDH) Lactase deficiency, congenital ( LCT) Lactase persistance[en.praenatal-medizin.de]

  • Alpers Syndrome

    acidosis, and strokelike episodes syndrome (MELAS) during recurrent status epilepticus ( 14 ).[ajnr.org] クスマウル Kussmaul respiration クスマウル大呼吸 AdolfKussmaul (1822-1902) Germaninternist Kveim クベイム反応 Kveim reaction クベイム反応 MortenAnsgar Kveim (1892-1966) Norwegian pathologist Ladd[jams.med.or.jp] Developmental delays and cognitive dysfunction is present which manifests in the form of increased sleepiness, dementia and loss of concentration.[symptoma.com]

  • Acute Renal Failure

    Swiss Med Wkly. 2012 Aug 14;142:w13662. doi: 10.4414/smw.2012.13662. eCollection 2012. Author information 1 Pediatric Cardiac Anesthesia/Intensive Care Unit, Department of Pediatric Cardiology and Cardiac Surgery, Bambino Gesù Children's Hospital, Rome, Italy. accaria.ricci@gmail.com Abstract The term acute kidney injury (AKI)[…][ncbi.nlm.nih.gov]

    Missing: Cognitive Developmental Delay Persistent Lactic Acidosis