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Clozapine levels in hair reflect dosage and bind more to pigmented hair.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

A new method accurately measures clobetasol propionate in hair and skin.

Manage side effects of hepatitis C treatment with dose changes and medications, which may improve patient adherence and treatment success.

Certain gene variations increase the risk of alopecia areata in Koreans.

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

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

CTP-543 effectively promotes hair regrowth in adults with moderate to severe alopecia areata.

Diphenyl cresyl phosphate has low toxicity but can harm the liver, kidneys, adrenal glands, and testicles at high doses.

Finasteride increases P-glycoprotein activity in the liver and kidney.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

Suppressing ODC activity reduces tumor growth in hair follicles.

TYK2 inhibitors show promise for treating cancer and autoimmune disorders.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Cinacalcet may help treat hereditary vitamin D resistant rickets safely.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

Dihydroxyacetone in self-tanning lotion helped reduce sun-related skin issues in a woman with variegate porphyria.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Micelles can change cetirizine's ionization, affecting its effectiveness in treatments.

A mutation in the VDR gene affects hair cycling without needing ligand binding.