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T. Ferdousi

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Open access Oct 2026

Late-onset Hypogonadism: Current perspective on diagnosis, management and impact on healthy aging

Late-onset hypogonadism (LOH), also termed age-related testosterone deficiency, is a clinical and biochemical syndrome affecting aging men. It is characterized by persistent hypogonadal symptoms paired with low serum testosterone levels. Unlike classical organic hypogonadism, LOH stems from a complex multifactorial mec...

T. Ferdousi · 0 citations
Open access Oct 2026

46, XX disorder of sex development due to simple virilizing congenital adrenal hyperplasia: A case report

Background: Congenital adrenal hyperplasia is an important cause of 46,XX disorder of sex development and may present with virilized external genitalia at birth. Early recognition is essential to guide sex assignment, endocrine evaluation, counselling, and timely surgical planning. Case summary: A 4-year-old child pres...

Md. Rakibur Rahman, Indrajit Prasad, M. Saifuddin et al. · 0 citations
Open access Oct 2026

A striking lipid phenotype: A case of homozygous familial hypercholesterolemia

Background: Homozygous familial hypercholesterolemia (HoFH) is a rare, severe genetic disorder characterized by markedly elevated low-density lipoprotein (LDL) cholesterol and premature atherosclerotic cardiovascular disease. Early recognition is crucial, as timely diagnosis and aggressive lipid-lowering therapy can si...

Murshida Rahman Rumi, Shajneen Alam, Tamanna Alam et al. · 0 citations

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