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Growth hormone levels affect hair growth and loss, with too much causing excess hair and too little leading to hair loss.

The conclusion is that early diagnosis of skin signs linked to diseases like Lupus, Dermatomyositis, and Rheumatoid Arthritis is crucial to prevent serious complications.

Eating fewer calories may slow skin aging and improve skin health through various biological changes.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Botulinum toxins are safe for various medical and cosmetic uses, but more research is needed for long-term safety and effectiveness in hair growth treatments.

Choosing the right method to separate skin layers is key for good skin cell research.

Skin, hair, and nail changes can help detect eating disorders early.

Six genetic conditions are often linked to complete scalp hair loss in children.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

Thyroid hormone may speed up wound healing and hair growth, but more research is needed to understand its role in skin repair and use as a treatment.

Markers help differentiate between apocrine and eccrine sweat glands to identify sweat gland tumors.

The term "porokeratotic adnexal ostial nevus" is proposed to unify overlapping skin conditions involving eccrine and hair follicles.

Human sweat glands have a type of stem cell that can grow well and turn into different cell types.

Enlarged sweat gland ducts may indicate scarring hair loss.

An adult with a rare skin condition improved with tazarotene treatment.

VEGFR-2 is active in hair follicles, sebaceous glands, sweat glands, and skin on the human scalp.

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

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Two cases of a rare skin condition were successfully treated with laser therapy, offering a non-surgical treatment option.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

Researchers found a new way to isolate sweat glands from the scalp for study and culture.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

Eccrine gland activity may be linked to alopecia areata.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

A 90-year-old woman's hand lesion was a rare, aggressive skin cancer treated successfully with surgery.

Plaque-type herpetic folliculitis affects eccrine glands.

A rare case of scleredema in a diabetic woman showed loss of sweat glands, causing heat strokes, with treatment only slightly improving symptoms.

Terbinafine quickly builds up in skin and hair, staying effective for over 3 weeks.

The conclusion is that fat tissue in the skin is a new finding in Frontal fibrosing alopecia and may contribute to hair follicle and muscle degeneration.

Small white dots on the scalp seen with a dermoscope correspond to sweat ducts and vary with different hair disorders.