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Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Hairless gene not strongly linked to baldness.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

Cantú syndrome may be linked to pituitary adenomas.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Women with congenital adrenal hyperplasia have lower fertility, but with proper treatment, they can conceive successfully.

A new mutation in the HR gene causes hair loss in a specific family.

Dihydrotestosterone treatment can help penis growth in boys with 5α-reductase deficiency but doesn't fully normalize size after puberty.

Minoxidil 5% solution significantly improved hair density in a girl with loose anagen hair syndrome over 28 months, with no side effects.

Vitamin D receptor helps control hair growth genes in skin cells.

Laser hair-comb therapy doesn't improve male-pattern hair loss.

A gene mutation causes woolly hair in a Syrian patient.

No clear link between androgen receptor variation and hair loss, but more research needed.

Researchers found two new genetic variants linked to Alzheimer's disease.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Dutasteride and finasteride affect different cell types differently.

The Androgen Receptor could be a target for treating diseases like cancer, but more research is needed to confirm the effectiveness of potential treatments.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

Young women with nonclassic congenital adrenal hyperplasia may experience worse sexual function and mild depression compared to healthy women.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

We need better ways to test and understand SARMs to make safer and more effective treatments.

Finasteride caused blisters on hands and feet.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

Lipedematous alopecia involves a thickened scalp and hair loss, with limited effective treatments available.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.