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Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

RANK-RANKL signaling is essential for hair growth and skin health.

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Experts discussed hair care, genetic hair defects, hair loss treatments, nail surgery, lupus treatments, skin infections, and cosmetic allergies.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

The April 2016 JEADV issue covered various dermatology topics, including psoriasis, psoriatic arthritis, mTOR inhibitors, autoimmune diseases, photodynamic therapy, viral DNA in skin diseases, chronic hand eczema, and female hair loss.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

The man has a genetic skin condition called pachyonychia congenita.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The study found that the protein Dkk4 helps regulate hair growth by controlling Wnt signaling in mice.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The review concludes that accurate diagnosis of different types of hair loss requires proper biopsy techniques and understanding the hair growth cycle and underlying causes.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Researchers found WNT10A to be a key gene in developing goat hair follicles.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

Bimatoprost is safe and effective for improving eyebrow hair.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

Deleting the EDAR gene in Cashmere goats affects genes and proteins related to hair growth.

The study concludes that the EDA2R gene is activated by p53 during chemotherapy but is not necessary for chemotherapy-induced hair loss.

EGF and FGF help hair growth by affecting cell differentiation and fiber growth.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Light can turn on hair growth cells through a nerve path starting in the eyes.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.