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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

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Raman spectroscopy is promising for measuring and enhancing drug delivery in alopecia treatments.

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Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

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The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

The IBHRS is now operational.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

Certain genetic markers may increase or decrease prostate cancer risk.

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BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

CP-690,550 significantly reduced itching in patients with moderate-to-severe plaque psoriasis.

PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

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A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.