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Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Doctors linked maternal drinking to infant mortality and national decline, leading to public awareness and changes in law.

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.

The document suggests a possible connection between rapid weight loss and hair loss, and reports a case of skin condition improvement after stopping acne medication.

The meeting discussed various skin conditions, treatments, and unusual cases, highlighting the effectiveness of tetracycline in treating rosacea.

Dermatological conditions are complex and treatments often have mixed results.

Dermal stem cells help regenerate hair follicles and heal skin wounds.

Endoscopic forehead and brow lifting safely and consistently improves aged eyebrows, but may have complications.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

Coix seed extract helped resolve onycholysis in an elderly woman.

Blocking a protein called CXXC5 with a specific peptide can stimulate hair regrowth and new hair growth in wounds.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Merkel cells and Langerhans cells in hair follicles are closely connected and may interact.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

Identified genes linked to male-pattern baldness may help develop new treatments.

Cationic and nonionic surfactants provide better color intensity and resistance for semi-permanent hair dye than anionic surfactants.

The Hedgehog Signaling Pathway is important for skin and hair development and skin cancer treatment, but more research is needed to understand it fully.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

Dr. SKS Hair Booster Serum is safe and effective for reducing hair fall and promoting hair growth.

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Lanceolate complexes in mouse hair follicles are essential for touch and depend on specific cells for maintenance and regeneration.

Human stem cells can help form hair follicles in mice.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

Cat claws stay sharp by shedding their outer layer through microcracks formed during activities.