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Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Mutation in hairless gene may increase hair loss risk.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

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

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Mutation in hairless gene may increase hair loss risk.

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

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

Early-onset baldness is linked to genetics, lifestyle, and can indicate higher risk for heart and metabolic diseases, and affects mental health.

The study suggests that hypothyroidism may cause alopecia areata.

Immune cells are essential for early hair and skin development and healing.

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

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

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

Activating Wnt in skin cells controls the number of hair follicles by directing cell movement and fate.

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

Early signs of PCOS in girls, like irregular periods and polycystic ovaries, suggest a need for early diagnosis and intervention to prevent further health issues.

Keratin proteins are crucial for hair structure and strength.

Epidermal stem cells have various roles in skin beyond just maintenance, including forming specialized structures and aiding in skin repair and regeneration.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

Skin's epithelial stem cells are crucial for repair and maintenance, and understanding them could improve treatments for skin problems.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

Dermoscopy is a useful tool for identifying features of skin conditions, but more research is needed to define its role in dermatology.

Some brain cancer cells avoid immune system detection, and certain treatments could target this to slow their growth; also, certain fat cell precursors help regenerate hair and skin after injury.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Understanding where cancer cells come from helps create better prevention and treatment methods.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.