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A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

Human skin models are essential for studying skin's sensory, immune, and nervous system interactions.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

The role of certain genes in skin cell development may be linked to psoriasis, but the connection is unclear.

A new mouse mutation causes skin and hair defects due to a gene change.

Chick embryo extract helps rat hair follicle stem cells potentially turn into Schwann cells, important for the nervous system.

Skin changes can help identify eating disorders early.

A rare pituitary tumor in an 18-year-old male caused hormonal issues and vision loss, requiring surgery and further treatment.

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.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

The document reports the first Brazilian case of a girl with Becker nevus syndrome, characterized by skin changes, breast underdevelopment, and scoliosis.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

Hydrogel surface properties affect mouse embryoid body differentiation.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

Keratins are crucial for tissue strength, and mutations in keratin genes can lead to various diseases, highlighting the need for targeted therapies.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

Oxidative stress contributes to hair graying and loss as we age.

Certain drugs can cause early hair growth in mice by affecting the nerves.

Hair ages due to various factors and treatments like minoxidil and finasteride can help, but more research and better public awareness are needed.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

Keratin gene mutations cause various skin and hair disorders, but new research offers hope for future treatments.

Increasing zinc intake improved skin and hair symptoms in a rare genetic disorder.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.