Publications by authors named "T Pasqualini"

Article Synopsis
  • 21-hydroxylase deficiency is a leading cause of Congenital Adrenal Hyperplasia and presents in classical (severe) and nonclassical (mild) forms, with different genetic variants affecting patients across populations.
  • This study examined the CYP21A2 gene defects in a large group of 628 Argentine patients, detailing genetic variations and their frequency among classical and nonclassical forms, while also analyzing family members and partners.
  • Key findings highlighted the frequent variants identified, the correlation between genotype and clinical manifestations, and the identification of rare and novel mutations, contributing to a better understanding of this condition in the studied population.
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The aim of the current study was to search for the presence of genetic variants in the CYP21A2 Z promoter regulatory region in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Screening of the 10 most frequent pseudogene-derived mutations was followed by direct sequencing of the entire coding sequence, the proximal promoter, and a distal regulatory region in DNA samples from patients with at least one non-determined allele. We report three non-classical patients that presented a novel genetic variant-g.

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Although corticoid replacement is recommended for those late-onset adrenal hyperplasia with clinical manifestations, asymptomatic patients do not need treatment. We describe clinical features at diagnosis, treatment, and growth till adult- height, in 4 boys. At diagnosis, age ranged from 9.

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Normal testicular physiology results from the integrated function of the tubular and interstitial compartments. Serum markers of interstitial tissue function are testosterone and insulin-like factor 3 (INSL3), whereas tubular function can be assessed by sperm count, morphology and motility, and serum anti-Müllerian hormone (AMH) and inhibin B. The classical definition of male hypogonadism refers to testicular failure associated with androgen deficiency, without considering potential deficiencies in germ and Sertoli cells.

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The aim of the study was to establish the characteristics of presentation of 94 patients with Kinelfelter's syndrome (KS) referred to the endocrinologist at different ages. The diagnosis of KS was more frequent in the age group between 11 and 20 years (46.8%).

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