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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.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

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.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

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

Dupilumab helped improve skin and prevent new lesions in a child with a rare immune disorder and severe eczema.

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.

Long-term use of androgens can help manage Hereditary Angioedema (HAE) but may cause serious side effects, so alternative treatments with fewer side effects are being considered.

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.

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.

Swiss experts recommend specific guidelines for diagnosing and treating hidradenitis suppurativa to improve patient care.

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

FGF13 gene changes cause excessive hair growth in a rare condition.

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.

The document concludes that Hidradenitis suppurativa is often underdiagnosed, lacks definitive treatment, and requires better awareness and management strategies.

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