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PRP with microneedling improves hair growth and patient satisfaction more than injections for androgenetic alopecia.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Exosome treatment safely increases hair density in male patients with androgenetic alopecia.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

Minoxidil improved hair growth in a child with a rare genetic disorder.

Hypertrichosis lanuginosa causes excessive fine hair growth, often linked to genetics or cancer, with limited treatment options.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A 15-year-old girl has a benign skin tumor on her neck.

Female pattern hair loss is different from male pattern hair loss and has unclear genetic causes.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Msx2 deficiency in mice leads to bone growth and organ development problems.

Only a few hair-specific keratins are linked to inherited hair disorders.

Dlx3 is essential for hair growth and regeneration.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Hair can be damaged by daily routines, but protein-based products can protect and improve it.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

Hair graying may be caused by stem cell depletion from stress or melanocyte damage.

The 810-nm diode laser improves skin texture in keratosis pilaris but not redness.

Nilotinib can cause keratosis pilaris, a skin condition.

Genetics and nutritional deficiencies are key factors in premature graying of hair.

Dermoscopy helps accurately diagnose temporal triangular alopecia, avoiding unnecessary treatments.