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93 Possible Causes for Cardiomyopathy, Green Jaundice, Pediatric Disorder

  • Hereditary Hyperphosphatasia

    Hyperandrogenism Due to Cortisone Reductase Deficiency HYP625 Hyperbilirubinemia, Rotor Type HYP236 HBLRR Hyperbilirubinemia, Transient Familial Neonatal HYP766 HBLRTFN Hyperbiliverdinemia[malacards.org] 1A 6 Dilated Cardiomyopathy 1Aa 6 Dilated Cardiomyopathy 1BB 1 Dilated Cardiomyopathy 1C 6 Dilated Cardiomyopathy 1CC 6 Dilated Cardiomyopathy 1D 4 Dilated Cardiomyopathy[preventiongenetics.com] Bone Histomorphometry 383 Chapter 17 A Diagnostic Approach to Skeletal Dysplasias 403 Chapter 26 Familial Hypophosphatemia and Related Disorders 699 Chapter 27 Hereditary[books.google.it]

  • Acute Catarrhal Tonsillitis

    Skimmed milk and buttermilk, lean meat, soups, bread, and green vegetables may be used.[mcmillinmedia.com] Rare but serious complications after strep tonsillitis are the glomerulonephritis and rheumatic fever, which triggers cardiomyopathies and rheumatic-like joint pain [69].[egms.de] In toxemic jaundice the main object of treatment must be the removal from the system of the poison that is causing the trouble.[mcmillinmedia.com]

  • Limb-Girdle Muscular Dystrophy Type 1H

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com] Disorders E-2903 168 Measurement of Health Outcomes in Pediatric Neurologic Disorders E-2910 169 The Influence of Computer Resources on Child Neurology E-2918 170 Education[books.google.com]

  • Congenital Hemihypertrophy

    […] to 21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1-SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] Bilateral adrenal pheochromocytomas have also been described in patients with Beckwith–Wiedemann syndrome (BWS), a pediatric overgrowth disorder, usually presenting with hemihypertrophy[edmcasereports.com] Dermatology; a textbook of skin disorders of childhood and adolescence.[olox.pro]

  • Cyanotic Congenital Heart Disease

    In these patients, the coincidence of cyanosis and jaundice caused an atypical green-appearing cutaneous discoloration which masked the early clinical detection of biliary[ncbi.nlm.nih.gov] A recent case report describes the anesthetic management of an AC in a patient with cardiomyopathy and low cardiac output 15.[f1000research.com] […] hypertrophy on ECG Common causes of CHF in the pediatric patient include structural causes such as VSD, ASD, Aortic Stenosis and PDA as well as other causes such as SVT, AV block, cardiomyopathy[emergencymedicinecases.com]

  • Glutamate Formiminotransferase Deficiency

    […] dystrophy type III Granular-lattice corneal dystrophy Granulomatosis with polyangiitis Gravidic intrahepatic cholestasis Gray platelet syndrome Gräsbeck-Imerslund disease Green[csbg.cnb.csic.es] […] hypertrophic cardiomyopathy 7 Familial hypertrophic cardiomyopathy 6 Familial hypertrophic cardiomyopathy 4 Familial hypertrophic cardiomyopathy 3 Familial hypertrophic cardiomyopathy[amp.pharm.mssm.edu] […] hematologic disorders, including newly recognized ones.[books.google.com]

  • Edema of the Newborn

    Definition Jaundice is a yellowing of the skin and/or whites of the eyes caused by high levels of bilirubin—a dark yellow-green or orange-red pigment—in the blood.[healthofchildren.com] Hydrops is not a common manifestation of neonatal liver disease unless there is associated cardiomyopathy or multiorgan failure.[healio.com] Pediatr Ann. 1976;5:518–35. 7. Nazif MM, Davis H, McKibben DH, Ready MA. Oral disorders. In: Zitelli BJ, Davis HW, eds. Atlas of pediatric physical diagnosis. 2d ed.[aafp.org]

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    […] to 21-hydroxylase deficiency, 201910 UGT1A1 Hyperbilirubinemia, familial transcient neonatal, 237900 SLCO1B1-SLCO1B3 Hyperbilirubinemia, Rotor type, digenic, 237450 BLVRA Hyperbiliverdinemia[gsdseq.ir] , Dilated, 1ee MYH6 Cardiomyopathy, Dilated, 1g TTN Cardiomyopathy, Dilated, 1y TPM1 Cardiomyopathy, Familial Hypertrophic, 1 MYH6 Cardiomyopathy, Familial Hypertrophic, 14[selfdecode.com] Pediatric Endocrinology: Growth, adrenal, sexual, thyroid, calcium, and fluid balance disorders. CRC Press. pp. 15–. ISBN 978-1-4200-4270-2. Retrieved 7 January 2011.[en.wikipedia.org]

  • Hypertrichotic Osteochondrodysplasia

    Cases 401948 Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency 4 Cases 168588 Hyperandrogenism due to cortisone reductase deficiency 11 Cases 276405 Hyperbiliverdinemia[azkurs.org] Diseases related with Cardiomyopathy and Short phalanx of finger In the following list you will find some of the most common rare diseases related to Cardiomyopathy and Short[mendelian.co] Frieden, two of the most important names in the fields of dermatology and pediatrics.[books.google.com]

  • Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] Associated with more severe cardiomyopathy Progression: Slow Exercise intolerance (50%) Fatigue & Myalgia: Occasional patient Muscle hypertrophy : Calves Rhabdomyolysis :[neuromuscular.wustl.edu] Pediatrics. 105 (1): e10. doi : 10.1542/peds.105.1.e10. PMID 10617747.[en.wikipedia.org]

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