Parathyroid hormone resistance and B cell lymphopenia in propionic acidemia |
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Authors: | TA Griffin RW Hostoffer K-Y Tserng DJ Lebovitz CL Hoppel JL Mosser D Kaplan DS Kerr |
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Affiliation: | Department of Pediatrics, Case Western Reserve University School of Medicine. Cleveland, OH. USA;Department of Nutrition, Case Western Reserve University School of Medicine. Cleveland, OH. USA;Department of Medicine, Case Western Reserve University School of Medicine. Cleveland, OH. USA;Department of Pathology, Case Western Reserve University School of Medicine. Cleveland, OH. USA |
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Abstract: | The mechanisms of hypocalcemia, recurrent infections and hypogammaglobulinemia associated with metabolic decompensation of propionic acidemia due to propionyl-CoA carboxylase deficiency have not been defined. A 7-week-old infant with this disorder presented with severe hypocalcemia and B cell lymphopenia during an episode of metabolic acidosis and hyperammonemia. Hypocalcemia (1.1 mmoll 1) was associated with elevated serum intact parathyroid hormone (122 ng 1 1), hyperphosphatemia, hypophosphaturia and hypercalcuria, indicating parathyroid hormone resistance. B cell lymphopenia (20 cells μl-1) was associated with transient neutropenia, anemia and subsequent hypogammaglobulinemia (IgG < 294mgdl-1, IgM < 8mgdl-1, IgA < 8mgdl 1), while T cells were normal. Parathyroid hormone resistance and B cell lymphopenia resolved following treatment with hemodialysis, diet and carnitine. These complications may be due to interference with parathyroid hormone renal tubular action and B cell maturation/proliferation by accumulated organic acids. |
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Keywords: | B lymphocytes carnitine hypocalcemia immunoglobulins lymphocytopenia parathyroid hormone propionic acid propionyl—CoA carboxylase |
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