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Author

Md. Saddam Hossain

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Open access Oct 2026

The enigma unfolds: ARMC5-associated primary bilateral macronodular adrenal hyperplasia in a young man

Background: Primary bilateral macronodular adrenal hyperplasia (PBMAH) is a rare cause of ACTH-independent Cushing syndrome. Germline pathogenic ARMC5 variants are among the most well-established genetic causes and are associated with variable penetrance and clinical expression. Diagnosis of PBMAH can be difficult and...

N. Akter, Tazkia Nur, Abdullah Al Noman Bhuiyan et al. · 0 citations
Open access Oct 2026

From hormonal failure to fatherhood: Natural conception after targeted endocrine treatment of secondary hypogonadism

Background: Secondary hypogonadism is a potentially reversible cause of male infertility but may remain unrecognized during routine infertility evaluation. Appropriate endocrine assessment and targeted treatment of hypothalamic-pituitary-gonadal dysfunction may restore spermatogenesis and enable biological fatherhood....

Md. Saddam Hossain, S. Jahan · 0 citations

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