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The DLQI is a key tool for measuring quality of life in dermatology.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

A specific gene variant may increase the risk of developing Alopecia Areata.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

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

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Different gene mutations cause different types of ichthyosis, with some new mutations found.

MicroRNAs and AI can improve cashmere goat hair quality and aid in hair disorder diagnosis.

New LSS gene variants help understand congenital hypotrichosis 14 better.

Iron deficiency can cause psychiatric symptoms that improve with proper treatment.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

A single robotic system can accurately harvest and implant hair grafts, showing promise for real-world use.

Mutations in the HOXC13 gene cause hair and nail development issues.

A gene variant causes a skin and hair disorder by disrupting protein balance.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Some women with PCOS have rare genetic variants linked to the condition.

Dihydroartemisinin could be a versatile cosmetic ingredient but needs more research and development.

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

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Electrophoresis can effectively analyze hair proteins for forensic use, even after cosmetic treatments and up to 2 years of weathering.