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Women with PCOS and polycystic ovaries have higher male hormone levels and more insulin resistance, especially if they are overweight.

Necrobiosis lipoidica may need new criteria for accurate diagnosis due to similarities with another condition.

The skin of both rat strains showed similar lectin binding patterns.

Different types of androgens bind differently to two receptors, AR1 and AR2, in Atlantic croaker's brain and ovarian tissues, suggesting these receptors may control different androgen actions in fish.

Key genes IRF2BP2 and EGFR are linked to Hetian sheep's double-coat fleece.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

The improved genome of the African spiny mouse helps study its tissue regeneration.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Hormonal changes during the reproductive cycle may cause seasonal skin problems in captive female fossas.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Anorexia nervosa can harm fertility and increase pregnancy risks.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Lower 2D:4D ratio and older age increase the risk of severe hair loss in men.

Misuse of topical steroids worsens skin infections, causing unusual and severe symptoms.

Agoutis in captivity have more resting (telogen) hairs than growing (anagen) hairs, regardless of season or gender.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

TTD symptoms vary widely, requiring thorough evaluations.

Indian women with PCOS may need different ultrasound criteria for diagnosis than current standards.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Inhaled steroids in children may cause excessive hair growth and not always go away after stopping the medication.

A new gene mutation causes a rare type of hair loss.

Dermatophylosis sporadically affects adult sheep in Sertão da Paraíba, causing alopecic and crusty skin lesions.

Male infertility and genitourinary birth defects are often linked to genetic issues.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Epithelial elements in superficial angiomyxomas are non-neoplastic growths mimicking embryogenesis.