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Measuring 24-OHase induction helps identify defects in vitamin D processing and predict treatment response.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Overexpressing noggin in mice causes severe osteoporosis.

Topical tofacitinib helped a man with severe scalp condition after other treatments failed.

Frontal fibrosing alopecia is a complex condition with no definitive treatment.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Hair-shaft abnormalities can indicate neurological disorders, some of which are treatable.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

It's important to understand the differences between FMF and PFM in children.

Knocking out the FGF5 gene in sheep increased wool production and hair-follicle density.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

A girl with a rare skin condition improved after one month of treatment with acitretin.

Frontal fibrosing alopecia is increasing, especially in postmenopausal women, and treatment with finasteride can improve it.

Cosmetic treatments can replenish key amino acids in damaged hair, improving its strength and appearance.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

HLD10 can include increased body hair and Mongolian spots.

Biotinidase deficiency can be easily diagnosed and treated with biotin to prevent serious harm.

Netherton syndrome is a genetic skin disorder causing severe skin issues and requires careful treatment to protect the skin barrier.

Frontal fibrosing alopecia causes hairline recession and eyebrow loss in postmenopausal women.

A rare genetic mutation in the EGFR gene caused severe skin issues and other health problems in a Slovakian girl, who is now 4 years old and receiving care.

Netherton syndrome causes skin and hair issues, confirmed by "bamboo hair" under dermoscopy, with no cure but managed with topical treatments.

Tufted folliculitis is common in patients with folliculitis decalvans.

FER and TOR signaling help root hair growth in low temperature and low nitrate conditions.

Frontal fibrosing alopecia often occurs after menopause, with delayed diagnosis and possible links to certain medications and conditions.

Keratin is crucial for skin barrier formation and affects mitochondrial function.

TLR2 helps control hair growth and regeneration, and its reduction with age or obesity can impair hair growth.

Females with 5 alpha-reductase-2 deficiency have less body hair, no acne, normal fertility, and delayed menarche.

Noggin promotes skin tumors by activating certain cell signaling pathways.