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Retinoids are effective for various skin conditions and hair loss but have serious side effects, so low doses are recommended.

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

Chitin nanofibrils are better at stabilizing oil droplets in emulsions than cellulose nanofibrils.

Recognizing rare tumor combinations is crucial for accurate diagnosis and treatment.

Newborns with ichthyosis need specific care based on their skin type.

A new method was developed to accurately detect and measure 47 different drug ingredients in various products.

A rare case showed basal cell carcinoma and leiomyosarcoma coexisting, needing careful diagnosis and treatment.

Understanding embryologic layers improves skin disorder diagnosis and supports developing targeted therapies.

Vertical mergers can lead to collusion, advertising often peaks then declines, and incumbents can disrupt new competitors.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Some people with chronic hair loss may have thyroid autoimmunity.

The newborn's skin condition improved over time, leaving only lighter skin patches.

The newborn's skin blisters healed without scarring, leaving some light spots, and stopped forming after four months.

Skin patterns form through molecular signals and genetic factors, affecting healing and dermatology.

Treatment with moisturizers improved the skin condition of a girl with a rare genetic skin disorder.

A person had two different benign skin tumors, a trichoadenoma and melanocytic naevi, at the same time but in different places on the face.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Papain and bisulfite break down human hair by dissolving parts of it.

A new gene mutation linked to a skin condition was found in a Spanish family.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

Injecting triamcinolone into the eyebrow area may help eyelash regrowth in alopecia areata patients.

Fresh plasma transfusions did not help treat Leiner disease in an infant.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

The method using ionic liquid improves observation of cell structures with less damage.

EVAL membranes help create cell structures that can regrow hair follicles.

Human hair has more unsaturated fats inside than on the surface, and certain lipids may help bind the outer and inner layers together.