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Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Sarcoptic mange nearly wiped out vicuñas and guanacos in an Argentine park.