inosinic-acid and Gigantism

inosinic-acid has been researched along with Gigantism* in 1 studies

Other Studies

1 other study(ies) available for inosinic-acid and Gigantism

ArticleYear
Myoadenylate deaminase deficiency, hypertrophic cardiomyopathy and gigantism syndrome.
    Pediatric neurology, 1997, Volume: 17, Issue:1

    We report a 20-year-old man with gigantism syndrome, hypertrophic cardiomyopathy, muscle weakness, exercise intolerance, and severe psychomotor retardation since childhood. Histochemical and biochemical analysis of skeletal muscle biopsy revealed myoadenylate deaminase deficiency; molecular genetic analysis confirmed the diagnosis of primary (inherited) myoadenylate deaminase deficiency. Plasma, urine, and muscle carnitine concentrations were reduced. L-Carnitine treatment led to gradual improvement in exercise tolerance and cognitive performance; plasma and tissue carnitine levels returned to normal, and echocardiographic evidence of left ventricular hypertrophy disappeared. The combination of inherited myoadenylate deaminase deficiency, gigantism syndrome and carnitine deficiency has not previously been described.

    Topics: Adenosine Diphosphate; Adenosine Triphosphate; Adult; AMP Deaminase; Biopsy; Cardiomyopathy, Hypertrophic; Carnitine; Diagnosis, Differential; Gigantism; Humans; Inosine Monophosphate; Male; Muscle, Skeletal; Phenotype; Purine-Pyrimidine Metabolism, Inborn Errors

1997