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5,262 Possible Causes for Acidosis, Neonatal Hypoglycemia, Subsarcolemmal Accumulation of Normal Mitochondria

  • Neonatal Respiratory Distress Syndrome

    Blood gases show respiratory and metabolic acidosis in addition to hypoxia.[amboss.com] No death was recorded in newborns with TTN, neonatal hypoglycemia and neonatal anemia.[panafrican-med-journal.com] Would also see hypoglycemia in these infants (because pancrease producing a large amount of insulin in response to being bathed by maternal insulin).[quizlet.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Hereditary Fructose Intolerance

    Three aspects of this case expand the published literature on this syndrome: (1) Metabolic acidosis was found to be due to both lactic acidosis and proximal renal tubular[ncbi.nlm.nih.gov] Fructose-1,6-diphosphate deficiency is another form of fructose intolerance, which usually presents as neonatal hypoglycemia.[healthhype.com] Decreased tubular reabsorption of bicarbonate lowers the blood bicarbonate concentration and contributes to metabolic acidosis.[symptoma.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Addison's Disease

    Signs and symptoms include low blood pressure, nausea and vomiting, syncope, hypoglycemia, hyponatremia, hyperkalemia, a metabolic acidosis, lethergy, confusion, and convulsions[openanesthesia.org] We describe a case of Addison's disease who was initially misdiagnosed as a case of meningo-encephalitis subsequently renal tubular acidosis and finally Addison's disease.[ncbi.nlm.nih.gov] acidosis (increased blood acidity), also due to loss of the hormone aldosterone In suspected cases of Addison's disease, one needs to demonstrate that adrenal hormone levels[web.archive.org]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Glycogen Storage Disease Type 1

    Treatment of acute metabolic acidosis episodes [ edit ] The most significant acute problem in childhood is a vulnerability to episodes of metabolic acidosis precipitated by[en.wikipedia.org] However, several cases of FBG have been detected through neonatal screening of galactose levels.[orpha.net] Patients with type 1 glycogen storage disease can present during the neonatal period with lactic acidosis and hypoglycemia.[themedicalbiochemistrypage.org]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Methylmalonic Acidemia

    An inborn error of metabolism leading to chronic metabolic acidosis. Statistics from Altmetric.com This is a PDF-only article.[doi.org] Barkovich AJ, Ali F, Rowley HA et al (1998) Imaging patterns of neonatal hypoglycemia. AJNR 19:523–528 PubMed Google Scholar 30.[doi.org] Investigation documented the presence of a proximal renal tubular acidosis.[ncbi.nlm.nih.gov]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Accidental Hypothermia

    acidosis that result from physiologic attempts to compensate for the heat loss.[ncbi.nlm.nih.gov] The patient presented with a severe respiratory and metabolic acidosis which was corrected during cardiopulmonary bypass (CPB).[ncbi.nlm.nih.gov] The advantages of HD when compared with CBP are that it is (1) more widely and readily available, (2) less invasive, (3) less expensive, and (4) can correct associated acidosis[ncbi.nlm.nih.gov]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Carnitine Transporter Deficiency

    ., hepatomegaly ) Diagnosis Observation of cystine crystals in the cornea during slit lamp examination Progressive GFR Hypokalemia, hyponatremia, metabolic acidosis Confirmed[amboss.com] hypoglycemia and sudden death JOURNAL-OF-CLINICAL-INVESTIGATION.[malattierare.regione.veneto.it] Carnitine deficiency may cause muscle necrosis, myoglobinuria, lipid-storage myopathy, hypoglycemia, fatty liver, and hyperammonemia with muscle aches, fatigue, confusion,[msdmanuals.com]

  • Fetal Hypoxia

    […] biochemical signs of hypoxia and acidosis.[ncbi.nlm.nih.gov] Absent / Reverse End Diastolic Flow Risk to Neonate  More admissions to NICU  Increase ICH  Increase Anemia  Increase Hypoglycemia  Increase long term permanent neurological[slideshare.net] […] morbidities associated with growth restriction, including asphyxia, meconium aspiration, sepsis, hypoglycemia and malformations.[aafp.org]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Galactosemia

    acidosis and edema.[msdmanuals.com] , bleeding disorder, vomiting, diarrhea, failure to thrive, hypoglycemia, coagulopathy, hemolysis or renal tubular acidosis.[ncbi.nlm.nih.gov] The neonatal erythrocyte galactose-1-phosphate (Gal-1-P) peak level was increased in 90.8% (89/98) of patients (Table 2 ).[ojrd.biomedcentral.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Glycogen Storage Disease Type 6

    In less common forms of the disease, symptoms (particularly hypoglycemia and hepatomegaly) may be severe and patients may even develop metabolic (lactic) acidosis after meals[symptoma.com] Patients with type 1 glycogen storage disease can present during the neonatal period with lactic acidosis and hypoglycemia.[themedicalbiochemistrypage.org] Rare variants may cause muscle dysfunction, peripheral neuropathy, proximal renal tubule acidosis, or severe cardiomyopathy.[humpath.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria

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