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Blocking DGAT1 reduces oil gland size in mice and dogs, but only mice experience hair loss.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Hair loss in men is mainly caused by hormones and genes, and while current treatments can slow it down, they can't fully stop it.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Some women with PCOS have rare genetic variants linked to the condition.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Heredity and hormones cause common hair loss, and topical minoxidil is the first recommended treatment.

Alopecia areata is an autoimmune disease with genetic links, treatable with certain medications, and can affect mental health.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

Understanding skin structure and development helps diagnose and treat skin disorders.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

Any drug can cause skin reactions, but antibiotics, NSAIDs, and psychotropic drugs are more common, with some reactions being life-threatening.

Custom skincare can be made based on genes, fewer cats in Lublin have FeLV/FIV than national average, and studies also looked at small water bodies, river pollution, guppy growth, toxins in biochars, palm oil issues, and pumpkin seed oil for hair strength.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

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

A thorough initial check-up is essential before sperm banking to ensure the best chance of preserving good quality sperm.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

Afro-textured hair needs personalized care due to its unique genetic traits.

SFRP2 and PTGDS may be key factors in female hair loss.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

The Middle East and Africa need better data, treatment consensus, and support for Alopecia Areata.

Alopecia areata is complex, often recurring, and needs personalized treatment, especially with other health issues.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

Hidradenitis Suppurativa is likely an autoinflammatory disease, and better understanding its causes could improve treatments.

Acne vulgaris is a common skin condition that can cause low self-esteem and depression, and early treatment is important to prevent scarring.