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A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Certain RNAs may help diagnose alopecia areata by affecting keratin genes.

Iron deficiency causes hair loss by affecting hair differentiation and cycling.

Endoplasmic reticulum stress plays a key role in developing atherosclerosis.

Women with PCOS in Sicily show different levels of metabolic problems depending on their PCOS type, with obesity and abnormal lipid profiles being common.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

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

Anorexia nervosa may cause a hair defect called pili torti due to malnutrition and high vitamin A levels.

Mutations in the HOXC13 gene cause hair and nail development issues.

Skin problems are common in people with diabetes and controlling blood sugar can reduce these issues.

A 54-year-old woman experienced progressive hair loss starting in adolescence, leading to sparse scalp hair and almost no eyebrows or eyelashes.

A man with itchy skin lesions and weight loss was diagnosed with a rare skin condition linked to a pancreatic tumor.

The document suggests "anisotrichosis" as a new term for hair thickness variation in common baldness.

Moth-eaten alopecia is linked to various skin diseases and requires early treatment to prevent worsening.

The man has a disease causing skin patches, thickened nerves, and mild muscle weakness.

Para-aminobenzoic acid in hair supplements can cause autoimmune hepatitis.

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

Decanoic acid may help treat PCOS by reducing androgen levels and improving glucose sensitivity.

PCOS patients with autoimmune thyroid disease have lower DHEAS levels.

Anorexia nervosa can cause skin problems, which may help with early diagnosis and usually improve with treatment.

Obese women with PCOS are more likely to have fatty liver disease.

Ustekinumab treatment may reveal a genetic tendency for steatocystoma multiplex in psoriasis patients.

A baby with a rare metabolic disorder developed a rash not cured by zinc alone, likely due to both zinc and amino acid deficiencies.

A young woman with a rare hair loss condition improved with steroid and biotin treatment.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

New treatments for alopecia areata show promise but need ongoing use and have infection risks.

A Laotian man with unusual skin changes and multiple growths in his gut was diagnosed with Cronkhite-Canada Syndrome and improved with nutritional and immune-based treatments.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.