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A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Careful management of steroid use is crucial in pregnant women with bullous pemphigoid to avoid complications like Cushing syndrome.

Recognizing specific skin features helps diagnose and manage lupus erythematosus effectively.

Obesity and bariatric surgery can cause hair thinning and temporary hair loss due to nutritional deficiencies and stress.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A well-equipped resident's bag enhances clinical skills, preparation, confidence, and learning for junior doctors.

The document encourages attending the 2023 Dermatology Nurses' Association Convention.

Seborrheic dermatitis and dandruff are often treated with antifungal and anti-inflammatory medications, which can reduce symptoms and yeast growth on the scalp.

Skin changes during pregnancy are common, and non-invasive imaging is safe for monitoring these changes.

Hair loss can be managed with treatments like minoxidil, finasteride, and others, but there are still gaps in effectiveness and off-label usage is increasing.

A horse in Brazil had seasonal hair loss possibly linked to light exposure and melatonin levels.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

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

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Low-level laser therapy is safe and can increase hair growth for male and female pattern hair loss.

The mineralocorticoid receptor may play a role in skin and hair health and could be a new target for treating related disorders.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

The skin issues in the two dogs might be caused by infection or self-injury, not genetics.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

People with anhidrotic ectodermal dysplasia may get severe bronchitis if exposed to dust.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.