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A 20-year-old woman was found to have a rare ovarian tumor causing symptoms like acne and a low-pitched voice, which disappeared after the tumor was removed.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Adolescents and young adults with Prader-Willi syndrome show a range of sexual interests and behaviors.

Finger length ratios might predict risk for skin condition in males.

Early diagnosis and treatment of haemochromatosis are crucial for reversing organ damage and improving fertility.

Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

Some skin diseases and their treatments can negatively affect male fertility.

Triptorelin helps evaluate hormone production in Sertoli-Leydig cell tumors.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

CAL-PDT is safer and more effective for treating actinic keratosis on the scalp.

DHT deficiency may disrupt rat epididymis function by affecting estrogen receptors.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Genetic analysis is crucial for diagnosing ectodermal dysplasia syndromes, and new therapies may help improve skin issues.

Becker's Melanosis and Hypertrichosis mainly affects young males, causing brown skin patches and extra hair on one side of the upper body.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

Micro-CT helps identify suitable areas for surgical procedures based on blood vessel distribution in hypospadias-affected rats.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A man with Klinefelter syndrome had a leg ulcer that didn't heal well, even with treatment.

Insufficient androgen action in male fetuses can cause genital development issues due to genetic mutations or environmental chemicals.

Trichoscopy is a helpful tool for diagnosing Netherton syndrome.

A 17-year-old female with adrenogenital syndrome produces very high levels of androgens, which prevent complete feminization despite high estrogen doses.

Finasteride exposure in pregnancy causes genital abnormalities in male rats.

Females with 5 alpha-reductase-2 deficiency have less body hair, no acne, normal fertility, and delayed menarche.

People with Down's syndrome are more likely to have syringomas.