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61 Possible Causes for Biventricular Hypertrophy, Delayed Growth and Development, Pediatric Disorder

  • Patent Ductus Arteriosus

    A large PDA may be associated with signs of biventricular hypertrophy (BVH) and in those with pulmonary hypertension, right ventricular hypertrophy (RVH) may be present.[] In the patient with a large ductus arteriosus and elevated pulmonary artery pressure, signs of right atrial enlargement and biventricular hypertrophy are frequently present[] ECG is often normal in small or moderate PDA but there may be signs of left ventricular hypertrophy (LVH).[]

  • Endocardial Cushion Defect

    hypertrophy Chest X-ray Cardiomegaly with increased pulmonary vascular markings Treatment Close the atrial and/or ventricular septal defects with patch material and repair[] , three leaflets with cleft in left atrioventriular valve Cardiac Auscultation Pulmonary flow murmur Atrioventricular regurgitation Electrocardiogram Left axis deviation Biventricular[]

  • Tetralogy of Fallot

    […] the muscular ventricular septum, obstruction of the right ventricular outflow tract, and right ventricular hypertrophy [ 2 ].[] Complications may include: Delayed growth and development Irregular heart rhythms (arrhythmias) Seizures during periods when there is not enough oxygen Death from cardiac[] -- Child & Adolescent Psychiatric Disorders & Psychosocial Aspects of Pediatrics -- Child Abuse & Neglect -- Ambulatory & Office Pediatrics -- Immunization -- Normal Childhood[]

  • Noonan Syndrome

    Biventricular hypertrophy (BVH) is a disease state characterized by the thickening of the ventricle walls.[] Bone development is also delayed by 2 years.[] NS is one of the RASopathies, which are a class of pediatric disorders associated with genes that are members of the mitogen-activated protein kinase (Ras/ MAPK ) pathway.[]

  • Cryopyrin-Associated Periodic Syndrome

    Cardiac amyloidosis masquerading as biventricular hypertrophy in a patient with multiple myeloma. BMJ Case Rep. 2013 Jul 29. 2013: [Medline].[] Growth retardation and delay in the development of pubertal traits may be observed as a consequence of chronic inflammation.[] Author information 1 a Division of Pediatric Rheumatology, Reference Center for Autoinflammatory Disorders CEREMAI, Bicêtre Hospital, University of Paris SUD, Le Kremlin Bicêtre[]

  • Acyanotic Congenital Heart Disease

    AR, Aortic regurgitation; ASD, atrial septal defect; BP, blood pressure; BVH, biventricular hypertrophy; CDG, congenital disorders of glycosylation; CHD, congenital heart[] growth In other cases, the symptoms of a congenital heart defect may not appear until many years after birth.[] Sheila Gahagan 11 Crying and Colic 12Temper Tantrums 13 Attention-Deficit/Hyperactivity Disorder 14 Elimination Control 15Normal Sleep and Pediatric Sleep Disorders Section[]

  • Donohue Syndrome

    Less common clinical features were also present, such as atrial septal defect and biventricular hypertrophy, clotting disorders, abnormal liver function tests and nephrocalcinosis[] They will exhibit delayed bone growth and maturation, and difficulty in gaining weight and developing (failure to thrive).[] J Pediatr 32: 739, 1948 CrossRef Google Scholar 2. Donohue WL, Uchida I: Leprechaunism, euphemism for a rare familial disorder. J Pediatr 45: 505, 1954.[]

  • Glycogen Storage Disease Type 3

    The remaining 26 patients had other forms of cardiac hypertrophy (isolated septal, right ventricular or biventricular hypertrophy).[] If GSD III is not treated, babies can have low blood sugar, enlarged liver, muscle weakness, delayed growth and development, sleepiness and irritability.[] Glycogen Storage Disease Ia [G6PC]: Biochemical abnormalities such as very low glucose level leading to delayed growth/development presenting in infancy.[]

  • Glycogen Storage Disease

    hypertrophy Glycogen: Increased in myocardium Phosphorylase kinase activity: Absent in myocardium Respiratory Failure Pulmonary edema Macroglossia : Some patients Death:[] The continued presence of low blood sugar can eventually lead to delayed growth and development as well as abnormal levels of some metabolites (substances) in the blood and[] Inborn Errors of Metabolism with Hypoglycemia: Glycogen Storage Diseases and Inherited Disorders of Gluconeogenesis. Pediatr Clin North Am. 2018 Apr. 65 (2):247-265.[]

  • Phosphorylase Kinase Deficiency

    hypertrophy Glycogen: Increased in myocardium Phosphorylase kinase activity: Absent in myocardium Respiratory Failure Pulmonary edema Macroglossia : Some patients Death:[] In their youth, patients displayed hepatomegaly (92%), growth retardation (68%), delayed motor development (52%), hypercholesterolaemia (76%), hypertriglyceridaemia (70%),[] Completely updated, the new edition of this easy-to-reference text examines the physiological, biochemical, and genetic aspects of pediatric endocrine disorders.[]