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Biomedical subjects

S Di Giovanni

Publications and source records attributed to S Di Giovanni.

21 records · Page 2Linked to original sources

Endocrine and neuropsychological assessment in a child with a novel mutation of thyroid hormone receptor: response to 12-month triiodothyroacetic acid (TRIAC) therapy.

OBJECTIVE: To determine the endocrine, neuropsychological and genetic features of a child with resistance to thyroid hormone (RTH), and his response to long-term triiodothyroacetic acid (TRIAC) therapy. METHODS: Growth, thyroid function, and neuropsychology were assessed at baseline and during 12-month TRIAC therapy. Genetic analysis was performed by PCR and denaturing high performance liquid chromatography. RESULTS: The main clinical finding was the attention deficit-hyperactivity disorder (ADHD). A novel mutation in exon 10 (phenylalanine to isoleucine in codon 455) was found. Long-term TRIAC therapy was effective in the management of the endocrine and neuropsychological manifestations of the syndrome. CONCLUSIONS: ADHD was the only phenotypic manifestation of this novel mutation of thyroid hormone (TH) receptor. TRIAC is an effective and safe drug in the long-term treatment of children with RTH.

Child↗

Serum beta 2-microglobulin in patients with monoclonal gammopathies.

Beta-2-microglobulin concentrations were determined in serum samples from 45 patients with benign and malignant monoclonal gammopathies. In the group of patients suffering from multiple myeloma or Waldenström macroglobulinemia the mean beta 2-microglobulin level was significantly higher than in the group with monoclonal gammopathy of undetermined significance. Values above 3 mg/L were highly indicative of a neoplastic process and were observed in all the Waldenström patients and in greater than 90% of myeloma patients. No significant correlation was noticed between beta 2-microglobulin and monoclonal protein levels in any of the groups examined.

Adult↗

Pseudothrombocytosis and pseudoleukocytosis in a case of essential mixed cryoglobulinemia (type II).

Pseudothrombocytosis and pseudoleukocytosis occurred in a patient with essential mixed cryoglobulinemia (EMC) and atypical cutaneous ulcers, when the blood cell counts were estimated by the Model S Plus Coulter Counter. The spurious cell counts were found in serum as well as in plasma and whole blood, so the involvement of fibrinogen in this phenomenon is questioned. When timed serial counts were performed on whole blood at room temperature the highest value of WBCs was detected one hour after sample collection and that of platelets occurred at 6 hours, when leukocytosis had disappeared. Possible explanations for this phenomenon are offered.

Cell Count↗