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Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Wnt and Shh signaling are key in noggin-induced tumors, and blocking them can slow tumor growth.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

CCCA is a scarring hair disorder mainly affecting people of African descent, needing better awareness and treatment.

Targeting the HEDGEHOG-GLI1 pathway could help treat keloids.

A man's neck lump was a trichilemmal cyst, not cancer, and should be fully removed due to rare risk of becoming malignant.

Alopecia areata patients have higher levels of certain immune receptors, suggesting new treatment possibilities.

Some skin tumors from hair follicles and glands can be linked to genetic syndromes and may be benign or malignant.

Reproductive hormones play a crucial role in breast cancer development and treatment challenges.

Platelet-rich plasma is an effective and safe treatment for male pattern hair loss.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Dogs with dermatomyositis, especially Collies and Shetland Sheepdogs, need better treatments for their skin and muscle inflammation.

A man had a non-cancerous neck tumor related to hair follicles removed with no return of the tumor.

Excessive eyelash growth from erlotinib may indicate positive tumor response and help treat madarosis.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Leech therapy and Ayurvedic treatment can effectively regrow hair in recent Alopecia areata cases.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A 56-year-old man was diagnosed with Cronkhite-Canada Syndrome after showing symptoms like diarrhea, weight loss, and skin changes.

Premature greying of hair affects the social lives of medical students but not their self-esteem.

A child with rough nails also had hair loss and allergies.

Seborrheic dermatitis is influenced by diet, genetics, and psychological factors.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

Lichen Planopilaris is a hair loss condition best treated early with various medications, including hydroxychloroquine, to prevent permanent baldness.

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

Different nail disorders are treated by targeting their specific causes and using appropriate medications or protective measures.

Eating a lot of soy might lower the chance of early hair loss in men likely to get it.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Dermoscopy helped correctly diagnose a skin condition that was previously misidentified as a different hair loss disease.

Monilethrix causes short, fragile hair with no specific treatment available.