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Dupilumab helped improve skin and prevent new lesions in a child with a rare immune disorder and severe eczema.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Combination therapies for androgenetic alopecia work best but can have significant side effects and costs.

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

The document concludes that while white skin, nail, and mucosa diseases increase skin cancer risk, they are generally harmless, especially compared to darker pigmentation conditions.

Eruptive vellus hair cysts are often missed in diagnoses.

Botulinum toxin injections effectively relieve pain from cutaneous leiomyomas.

Protein analysis shows aging changes in scalp cell types from women.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Skin aging and cancer development are influenced by the competition between stem cells.

Human-induced stem cell-created skin models can help understand skin diseases by studying the skin's layers.

Low oxygen levels affect the behavior of certain proteins in human skin cells.

Different genes are linked to various types of hair loss.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Targeting the Smoothened receptor shows promise for treating certain cancers.

Future hair cosmetics will be safer and more effective.

Vitamin D receptor may help protect against UV-induced skin cancer.

Hair loss in middle-aged women is often linked to insulin resistance and a family history of hair loss, particularly from their fathers.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

Drug repositioning is a promising way to quickly develop new treatments, especially for rare diseases.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

The supplement significantly improves hair density and appearance in people with hair loss.

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

A man had a large, rare cyst in his mouth removed after 10 years, which fixed his swallowing and breathing problems.

Dihydrotestosterone and 5α-Reductase play a role in hair loss and prostate health, and finasteride can increase hair growth in men without affecting sperm production, but it doesn't work for postmenopausal women with hair loss.