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Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

A new compound shows promise as a topical treatment for hair loss.

Early diagnosis and haemodialysis can effectively treat thallium poisoning.

A man's scalp condition was misidentified as hair loss dots but was actually a common follicular disorder.

BDNF, TSH, fT4, anti-TPO, and 25-OH Vitamin D levels predict depression risk in patients with autoimmune thyroiditis and hypothyroidism.

A woman and her daughter had thallium poisoning from a herbal drink and rodenticide, causing hair loss and other symptoms.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Thallium poisoning can be identified through radiological signs and treated effectively with B.A.L.

Combining ciprofloxacin with other treatments may improve its effectiveness against resistant bacteria.

FGF5 gene mutations cause long hair in domestic cats.

Improving CRISPR/Cas systems can make gene editing more efficient and precise.

circRNA-1926 helps goat stem cells turn into hair follicles by affecting miR-148a/b-3p and CDK19.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Sansevieria and Dracaena are evolutionarily linked, and a specific gene marker can distinguish closely related species.

Certain gene changes and hormone levels are linked to female hair loss.

KRT71 gene variants may influence camel hair shape but don't fully explain it.

Metabolites and diet affect hair growth cycles in cashmere goats.

Cultural awareness in healthcare improves patient care and relationships.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

DNA methylation is essential for skin and hair follicle development, and could be a target for treating skin diseases.

Triangular temporal alopecia can occur in adults and should be correctly identified to prevent misdiagnosis.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

People from iodine-deficient areas are more likely to develop hypothyroidism when treated for multi-drug resistant tuberculosis.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Grafted human scalp samples on mice can produce human hair, useful for studying hair genetics.

Routine genetic testing is crucial for early diagnosis and better management of Turner’s syndrome with 21-hydroxylase deficiency.

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Apoptosis in hair follicles spreads through cell death signals, with stem cells slowing the process.

2-DG reduces seizures by enhancing brain inhibition through specific receptor activation.