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A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Extra virgin olive oil may boost the immune system and help fight infections like COVID-19.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Biomedical engineers are crucial for developing better treatments for chronic and autoimmune diseases.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The document is a detailed medical reference on skin and genetic disorders.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Proper care and diet are crucial to prevent health issues in gerbils.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Prurigo pigmentosa mainly affects middle-aged White and Asian women, often linked to a ketogenic diet, and is best treated with oral antibiotics.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

Knocking out certain genes in mice helps understand skin and hair growth problems.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Netherton's syndrome is linked to high IgE levels and unique skin and hair symptoms, and may improve with ammonium lactate lotion and allergy management.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Melatonin improved secondary hair growth in goats but didn't affect primary hair density or litter size.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Both HPSAM and PLS methods accurately measure minoxidil and tretinoin concentrations.

Betamethasone dipropionate reduced skin thickness, fish oil increased it, and combined treatment had no significant effect.

H-1 antihistamines may help with various skin conditions, but more research is needed to confirm their effectiveness.

The research shows that hydrogen bonds greatly affect the crystal structure of a Finasteride derivative.

Testosterone and dihydrotestosterone can slow down the growth of certain hair follicle cells.