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"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

The fractional carbon dioxide laser is a safe and effective treatment for alopecia areata and works better than betamethasone valerate cream alone.

The boy's scurvy symptoms improved with vitamin C treatment, highlighting the need for a balanced diet.

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

Nocturnal calcium infusions improved a boy's severe rickets without causing hair loss.

Diphencyprone initially increases mouse hair growth, then slows it, possibly due to changes in specific protein levels.

Breast cancer alters specific molecular structures in hair, which revert after cancer removal.

The nanoemulsion of Avicennia marina extract effectively fights dandruff.

High CCL11 levels may indicate poor response to baricitinib in severe alopecia areata.

UC.145 may be a new biomarker for predicting gastric cancer.

Acrodermatitis enteropathica is a rare inherited disorder causing skin issues, diarrhea, and hair loss.

Targeting cholesterol, fatty acids, fibrosis, and mast cells may help treat CCCA.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

Frontal fibrosing alopecia can affect African men and may be underdiagnosed.

PCE-DP brightens skin and promotes hair growth by enhancing cell growth and reducing melanin uptake.

Daprodustat, combined with PAβN, could be a new antibacterial treatment.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

A new compound, 3a, effectively fights prostate cancer better than finasteride.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

A 13-year-old boy with a rare scalp condition improved significantly with isotretinoin, minoxidil, oral steroids, and antiseptic shampoo.

Low testosterone levels may contribute to female pattern hair loss in men.

Diphencyprone increases Bcl-2 protein in patients with hair regrowth from alopecia areata.