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77 Possible Causes for Hepatomegaly, Postural Defect, X-Ray Abnormal

  • Amyloidosis

    Hepatic involvement is common, but the clinical manifestations are usually mild with hepatomegaly and an elevated alkaline phosphatase level.[] Flies carrying mutant variants, but not wild-type TTR, exhibit changes in wing posture, locomotor defects, and shortened life span.[] […] that presents to a cancer care provider with nephrotic range proteinuria, heart failure with preserved ejection fraction, non-diabetic peripheral neuropathy, unexplained hepatomegaly[]

  • Homocystinuria

    […] inborn error of metabolism of sulfur amino acids due to lack of the enzyme cystathionine synthase; it is characterized by homocystine in the urine and by mental retardation, hepatomegaly[] Skeletal X-rays may demonstrate tubular appearance of bones, especially elongation and thinning of long bones, with widening of the epiphyses and metaphyses.[] Many, if not all, patients have some type of hepatic involvement which may produce mild hepatomegaly with imaging characteristics and/or biopsied pathology of fatty infiltration[]

  • Mediastinal Neoplasm

    Hoarseness Symptoms of Horner’s syndrome (ptosis, miosis, decreased sweating) Facial/upper limb edema and venous distension in neck and upper limbs/chest Lymphadenopathy Hepatomegaly[] Furthermore, asymmetry of the thoracic-lumbar spinal region was observed, which at first assessment suggested a postural defect.[] When the chest x-ray is found to contain an abnormal shadow which blends with the mediastinum, a diagnosis of neoplastic disease is often entertained.[]

  • Right to Left Shunt

    Hepatomegaly is a common manifestation in Gaucher disease. In some patients with the disease, hepatic fibrosis and portal hypertension are observed.[] Postural cyanosis and angina pectoris following pneumonectomy: relief by closure of an interatrial septal defect.[] Chest x ray was normal and there were no ECG abnormalities.[]

  • Tuberculous Gumma

    In the prednisolone-treated group, there was a significantly rapid resolution of raised jugular venous pressure, hepatomegaly, and ascitis.[] • Stationary/progressive • Associated field defects 8. • h/o Pain • h/o Double vision • h/o Trauma • h/o fever , chills ,systemic symptoms • h/o cancer • h/s/o thyroid disease[] Chest x-ray revealed no abnormalities.[]

  • Left to Right Cardiac Shunt

    […] low cardiac output (poor perfusion, increased lactate, low mixed venous oxygen saturation, low cerebral oxygen saturation), and elevated central venous pressures (edema, hepatomegaly[] Postural cyanosis and angina pectoris following pneumonectomy: relief by closure of an interatrial septal defect.[] They may be noted on routine testing to have an abnormal chest x-ray or an abnormal EKG and may have atrial fibrillation.[]

  • Congenital Malformation of the Ribs

    751.69 Other anomalies of gallbladder, bile ducts, and liver Absence of: gallbladder, congenital liver (lobe) Accessory: hepatic ducts liver Congenital: choledochal cyst hepatomegaly[] Congenital Vertebral Defects The spinal column is the central structure in the vertebrate body from which stability, movement, and posture all derive.[] X-Rays may identify and characterize specific abnormalities, but x-rays do not display fascial plane anatomy.[]

  • Cardiac Asthma

    Typical signs: tachycardia, tachypnoea, pulmonary rales, pleural effusion, raised jugular venous pressure (JVP), peripheral oedema, hepatomegaly.[] Patients with chronic CHF and orthopnea have a considerable increase in airflow resistance upon adopting the supine posture associated with supine expiratory flow limitation[] MD was severe he was prescribed all medications for asthma but it dint help X ray revealed cardiomegaly Echo ECG Showed abnormal extra beats It was diagnosed as cardiac asthma[]

  • Transient Hyperammonemia of the Newborn

    Infant becomes floppy, FTT, hepatomegaly, macroglossia at 1 month Noted cardiomegaly and hard muscles on exam Type 2 glycogen storage Pompe Diagnosis?[] Diagnosis Often the clinical appearance of urea cycle defects mimics that of other inborn errors of metabolism.[] Imaging Besides the straightforward abnormalities of the extremities, plain X-ray examination reveals more profound skeletal abnormalities, including calcifications within[]

  • Cutis Laxa

    In a family with four infants born to the same consanguineous parents all children presented at birth with dysmorphic features, cutis laxa and hypertrichosis, hepatomegaly[] Dystonic posturing was discriminatory for PYCR1 and ALDH18A1 defects. Metabolic markers of mitochondrial dysfunction were found in one patient with PYCR1 mutations.[] Chest x-ray ( Figure 2 A) showed abnormalities of the contours of upper right border of the heart.[]

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